Description:
CHROMOSOME DELETION
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Repository
|
NIGMS Human Genetic Cell Repository
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| Subcollection |
Chromosome Abnormalities |
|
Cell Type
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Fibroblast
|
|
Transformant
|
Untransformed
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|
Race
|
White
|
|
Family Member
|
1
|
|
Relation to Proband
|
proband
|
|
Confirmation
|
Karyotypic analysis after cell line submission to CCR
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|
ISCN
|
46,XX,del(10)(:p13>qter)
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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
|
|
| Passage Frozen |
3 |
| |
| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
| |
| Cytogenetics |
Chromosome 10: DELETION Aneuploid Segment (-)10pter>10p13 |
| Remarks |
Developmental delay and dysmorphic features; parents both have normal karyotypes; see GM06936 Lymphoid |
| Passage Frozen |
3 |
| Split Ratio |
1:3 |
| Temperature |
37 C |
| Percent CO2 |
5% |
| 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 |
| Substrate |
None specified |
| Subcultivation Method |
trypsin-EDTA |
| Supplement |
- |
|
|