NA01580
DNA from Fibroblast
Description:
TRANSLOCATED CHROMOSOME
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Chromosome Abnormalities |
| Quantity |
50 µg |
| Quantitation Method |
Please see our FAQ |
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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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Sample Source
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DNA from Fibroblast
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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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maternal grandmother
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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(10;21)(10pter>10q26::21q21> 21qter;21pter>21q21::10q26>10qter)
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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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| Passage Frozen |
6 |
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
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| Cytogenetics |
Chromosome 10: TRANSLOCATION Breakpoint 10q26 t(10;21)10q26 |
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Chromosome 21: TRANSLOCATION Breakpoint 21q21 t(10;21)21q21 |
| Williams JD, Summitt RL, Martens PR, Kimbrell RA, Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21. Am J Hum Genet27:478-85 1975 |
| PubMed ID: 125542 |
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