Description:
TRANSLOCATED CHROMOSOME
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Chromosome Abnormalities |
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Cell Type
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Fibroblast
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Transformant
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Untransformed
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Race
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Black/African American
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Family Member
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2
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Relation to Proband
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mother
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Confirmation
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Karyotypic analysis after cell line submission to CCR
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ISCN
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46,XX,t(14;20)(p11.2;p11.1)[19]
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Species
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Homo sapiens
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Common Name
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Human
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Remarks
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|
| PDL at Freeze |
5.08 |
| Passage Frozen |
6 |
| |
| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
| |
| Cytogenetics |
Chromosome 14: TRANSLOCATION Breakpoint 14p11 t(14;20)14p11 |
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Chromosome 20: TRANSLOCATION Breakpoint 20p11 t(14;20)20p11 |
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Chromosome 9: INVERSION Breakpoint 9p12 inv(9)9p12 |
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Chromosome 9: INVERSION Breakpoint 9q12 inv(9)9q12 |
| Remarks |
Phenotypically normal |
| Emanuel BS, Zackai E, Mellman WJ, Aronson MM, Greene AE, Coriell LL, A (14;20) balanced translocation, 46, XX. Repository identification No. GM-982. Cytogenet Cell Genet21:174 1978 |
| PubMed ID: 657848 |
| Passage Frozen |
6 |
| Split Ratio |
1:2 |
| Temperature |
37 C |
| Percent CO2 |
5% |
| Percent O2 |
AMBIENT |
| Medium |
Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent |
| Serum |
15% fetal bovine serum Not inactivated |
| Supplement |
- |
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