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GM06936 LCL from B-Lymphocyte

Description:

CHROMOSOME DELETION
COPY NUMBER VARIATION (CNV) REFERENCE PANEL

Affected:

No Data

Sex:

Female

Age:

2 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Chromosome Abnormalities
dbGaP
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race White
Family Member 1
Relation to Proband proband
Confirmation Karyotypic analysis after cell line submission to CCR
ISCN 46,XX,del(10)(p13)[20]
Species Homo sapiens
Common Name Human
Remarks Developmental delay and dysmorphic features; parents both have normal karyotypes; see GM06937 Fibroblast; gene copy numbers: D10S17-1, D10S28-1, VIM-2, and D10S34-2

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Chromosome Analysis
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Chromosome Analysis
 
GENE MAPPING & DOSAGE STUDIES - CHROMOSOME 10 Mathew et al (Ann Hum Genet 54:121-129,1990) analyzed DNA from this 46,XX,del(10) cell line in Southern blot hybridization experiments using a number of chromosome 10 markers to determine the copy numbers present. The following results were obtained: D10S17 (pter>p13) - 1 copy, D10S28 (pter>p13) - 1 copy, VIM (p13>p12) - 2 copies, and D10S34 (p12>p11) - 2 copies.
 
GENE MAPPING & DOSAGE STUDIES - CHROMOSOME 10 Mathew et al (Ann Hum Genet 54:121-129,1990) analyzed DNA from this 46,XX,del(10) cell line in Southern blot hybridization experiments using a number of chromosome 10 markers to determine the copy numbers present. The following results were obtained: D10S17 (pter>p13) - 1 copy, D10S28 (pter>p13) - 1 copy, VIM (p13>p12) - 2 copies, and D10S34 (p12>p11) - 2 copies.
 
CNVPANEL For more information click here:CNVPANEL01
 
CNVPANEL For more information click here:CNVPANEL01
 
Cytogenetics Chromosome 10: DELETION Aneuploid Segment (-)10pter>10p13

Phenotypic Data

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Remarks Developmental delay and dysmorphic features; parents both have normal karyotypes; see GM06937 Fibroblast; gene copy numbers: D10S17-1, D10S28-1, VIM-2, and D10S34-2

Publications

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Nyaga DM, Tsai P, Gebbie C, Phua HH, Yap P, Le Quesne Stabej P, Farrow S, Rong J, Toldi G, Thorstensen E, Stark Z, Lunke S, Gamet K, Van Dyk J, Greenslade M, O'Sullivan JM, Benchmarking nanopore sequencing and rapid genomics feasibility: validation at a quaternary hospital in New Zealand NPJ genomic medicine9:57 2024
PubMed ID: 39516456
 
Tan VJ, Liu T, Arifin Z, Pak B, Tan ASC, Wong S, Khor CC, Yang H, Lee CG, Huang Z, Choolani MA, Chong SS, Third-Generation Single-Molecule Sequencing for Preimplantation Genetic Testing of Aneuploidy and Segmental Imbalances Clinical chemistry9:57 2023
PubMed ID: 37477572
 
Walters-Sen L, Neitzel D, Bristow SL, Mitchell A, Alouf CA, Aradhya S, Faulkner N, Experience analysing over 190,000 embryo trophectoderm biopsies using a novel FAST-SeqS preimplantation genetic testing assay Reproductive biomedicine online44:228-238 2022
PubMed ID: 35039224
 
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
 
Schuffenhauer S, Lichtner P, Peykar-Derakhshandeh P, Murken J, Haas OA, Back E, Wolff G, Zabel B, Barisic I, Rauch A, Borochowitz Z, Dallapiccola B, Ross M, Meitinger T, Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2). Eur J Hum Genet6:213-25 1998
PubMed ID: 9781025
 
Daw SC, Taylor C, Kraman M, Call K, Mao J, Schuffenhauer S, Meitinger T, Lipson T, Goodship J, Scambler P, A common region of 10p deleted in DiGeorge and velocardiofacial syndromes. Nat Genet13:458-60 1996
PubMed ID: 8696341
 
Mathew CG, Wakeling W, Jones E, Easton D, Fisher R, Strong C, Smith B, Chin K, Little P, Nakamura Y, et al, Regional localization of polymorphic markers on chromosome 10 by physical and genetic mapping. Ann Hum Genet54 ( Pt 2):121-9 1990
PubMed ID: 1974407

External Links

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dbSNP dbSNP ID: 14209

Culture Protocols

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Split Ratio 1:4
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
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 -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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