GM06803
                                                
                                                LCL from B-Lymphocyte
                                                
                                                
                                             
                                            
                                                
                                                    
                                                         Description:
                                                    
                                                    
                                                         
                                                            
                                                            WILMS TUMOR 1; WT1 
                                                            
                                                            CHROMOSOME DELETION 
                                                            
                                                    
                                                 
                                                
                                                
                                                
                                                
                                             
                                         
                                     
                                    
                                        
                                            
                                            
                                            
                                            
                                                
                                                    
                                                        
                                                            
                                                            
                                                                
                                                                    
                                                                        | 
                                                                            Repository
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                                                                            NIGMS Human Genetic Cell Repository
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	| Subcollection | 
	Heritable Diseases Chromosome Abnormalities dbGaP | 
 
                                                                
                                                                
                                                                
	| Class | 
	Heritable Cancer Syndromes and other Cancers | 
 
                                                                
                                                                
                                                                
                                                                
                                                                    
                                                                        | 
                                                                            Biopsy Source
                                                                         | 
                                                                        
                                                                            Peripheral vein
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                                                                        | 
                                                                            Cell Type
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                                                                            B-Lymphocyte
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                                                                            Tissue Type
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                                                                            Blood
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                                                                        | 
                                                                            Transformant
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                                                                            Epstein-Barr Virus
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                                                                            Sample Source
                                                                         | 
                                                                        
                                                                            LCL from B-Lymphocyte
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                                                                        | 
                                                                            Race
                                                                         | 
                                                                        
                                                                            White
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                                                                        | 
                                                                            Relation to Proband
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                                                                            proband
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                                                                        | 
                                                                            Confirmation
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                                                                            Clinical summary/Case history
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                                                                        | 
                                                                            ISCN
                                                                         | 
                                                                        
                                                                            46,XY,del(11)(p14p12).arr 11p14.1p12(29201568-38196267)x1
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                                                                        | 
                                                                            Species
                                                                         | 
                                                                        
                                                                            Homo sapiens
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                                                                        | 
                                                                            Common Name
                                                                         | 
                                                                        
                                                                            Human
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                                                                        | 
                                                                            Remarks
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	| GENE MAPPING & DOSAGE STUDIES - CHROMOSOME 11 | 
	Gessler et al (Am J Hum Genet 44:486-495,1989) utilized 37 DNA probes which map to the WAGR region of chromosome 11 to define the WAGR gene loci and provide a high resolution map of this region. DNA from this cell culture showed reduced dosage, indicative of a heterozygous deletion, for at least some of the probes tested. | 
 
	|   | 
 
	| IDENTIFICATION OF SPECIES OF ORIGIN | 
	Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis and by Chromosome Analysis | 
 
	|   | 
 
                                                                
                                                                
                                                                
                                                                
	| Cytogenetics | 
	Chromosome 11: DELETION Aneuploid Segment  (-)11p13>11p11 | 
 
                                                                
                                                                
                                                                
                                                             
                                                         
                                                     
                                                 
                                                
                                                    
                                                        
                                                            
                                                            
                                                            
                                                                
	| Remarks | 
	Aniridia, mental retardation, hypogonadism, abnormal right kidney, high arched palate, microphallus, cryptorchidism, and dysplastic testes; 50% of normal mother's catalase act; 46,XY,del(11)(pter>p13:: p11.2>qter); 1 copy of catalase gene | 
 
                                                                
                                                             
                                                            
                                                            
                                                         
                                                     
                                                 
                                                
                                                    
                                                        
                                                            
                                                            
                                                            
                                                                
	| Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP, A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds G3 (Bethesda, Md)3:1143-9 2013 | 
 
	| PubMed ID: 23665875 | 
 
	|   | 
 
	| Gessler M, Thomas GH, Couillin P, Junien C, McGillivray BC, Hayden M, Jaschek G, Bruns GA, A deletion map of the WAGR region on chromosome 11. Am J Hum Genet44:486-95 1989 | 
 
	| PubMed ID: 2539014 | 
 
	|   | 
 
	| Marshall, Aniridia and the 11p13 deletion. Am J Hum Genet34:74A (1982):486-95 1982 | 
 
	| PubMed ID: 2539014 | 
 
                                                                
                                                             
                                                            
                                                         
                                                     
                                                 
                                                
                                                
                                                
                                                    
                                                        
                                                            
                                                            
                                                                
	| Split Ratio | 
	1:5 | 
 
	| Temperature | 
	37 C | 
 
	| Percent CO2 | 
	5% | 
 
	| Medium | 
	Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent | 
 
	| Serum | 
	15% fetal bovine serum Not Inactivated | 
 
	| Substrate | 
	None specified | 
 
	| Subcultivation Method | 
	dilution - add fresh medium | 
 
	| Supplement | 
	- | 
 
                                                                
                                                                
                                                             
                                                         
                                                     
                                                 
                                             
                                         
                                     
                                 
                                
                             
                         
                     
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