HM03226
High Molecular Weight DNA from Fibroblast
Description:
ANEUPLOID CHROMOSOME NUMBER - TRISOMY 9
ANEUPLOID CHROMOSOME NUMBER - TRISOMY
|
Repository
|
NIGMS Human Genetic Cell Repository
|
| Subcollection |
Chromosome Abnormalities
dbGaP |
| Alternate IDs |
GM17354 [ANEUPLOID CHROMOSOME NUMBER - TRISOMY 9] |
| Estimated Quantity |
5 µg - 20 µg |
| Product Specifications |
Please see our FAQ |
|
Cell Type
|
Fibroblast
|
|
Transformant
|
Untransformed
|
|
Sample Source
|
High Molecular Weight DNA from Fibroblast
|
|
Race
|
Black/African American
|
|
Ethnicity
|
TRINIDADIAN
|
|
Family Member
|
1
|
|
Relation to Proband
|
proband
|
|
Confirmation
|
Karyotypic analysis after cell line submission to CCR
|
|
ISCN
|
47,XY,+del(9)(9p13.1)mat.arr 9p24.3p13.1(36586-40085483)x3
|
|
Species
|
Homo sapiens
|
|
Common Name
|
Human
|
|
Remarks
|
|
| Passage Frozen |
2 |
| |
| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
| |
| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
| |
| Cytogenetics |
Chromosome 9: ANEUPLOID Aneuploid Segment (+)9pter>9q11 |
|
Chromosome 9: ANEUPLOID Trisomic Segment 9pter>9q11 |
|
Chromosome 9: DELETION Aneuploid Segment (+)9pter>9q11 |
|
Chromosome 9: DELETION Trisomic Segment 9pter>9q11 |
| Remarks |
Multiple malformations and mental retardation; see GM05067A Lymphoid |
| 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 |
| |
| Zhao X, Li C, Paez JG, Chin K, Janne PA, Chen TH, Girard L, Minna J, Christiani D, Leo C, Gray JW, Sellers WR, Meyerson M, An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays. Cancer Res64(9):3060-71 2004 |
| PubMed ID: 15126342 |
| |
| Zhou X, Cole SW, Hu S, Wong DT, Detection of DNA copy number abnormality by microarray expression analysis Human genetics114:464-7 2004 |
| PubMed ID: 14872338 |
| |
| Zhou X, Mok SC, Chen Z, Li Y, Wong DT, Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array Human genetics115:327-30 2004 |
| PubMed ID: 15290239 |
| |
| Porterfield BW, Pomykala H, Maltepe E, Bohlander SK, Rowley JD, Diaz MO, The use of methylthioadenosine phosphorylase activity to select for human chromosome 9 in interspecies and intraspecies hybrid cells [published erratum appears in Somat Cell Mol Genet 1994 May;20(3):249] Somat Cell Mol Genet19:469-77 1993 |
| PubMed ID: 7507266 |
| |
| Su TS, Nussbaum RL, Airhart S, Ledbetter DH, Mohandas T, O'Brien WE, Beaudet AL, Human chromosomal assignments for 14 argininosuccinate synthetase pseudogenes: cloned DNAs as reagents for cytogenetic analysis. Am J Hum Genet36:954-64 1984 |
| PubMed ID: 6093508 |
|
|