| PubMed ID |
|
25903014 |
Publish Date |
|
2015 Apr |
| Journal |
|
Journal of Hematology & Oncology |
Species |
|
Homo sapiens |
| Disease Type |
|
Acute lymphoblastic leukemia |
Technology |
|
SNP Array |
| Case Number |
|
1 |
Raw Data |
|
|
| Title |
|
Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A |
| Authors |
|
Karrman K, Castor A, Behrendtz M, Forestier E, Olsson L, Ehinger M, Biloglav A, Fioretos T, Paulsson K, Johansson B |
| Affiliation |
|
Department of Clinical Genetics, University and Regional Laboratories, Region Skane, SE-221 85, Lund, Sweden |
| Chromothripsis Definition |
|
Close-by breakpoints: 28
Copy number states: 2
Fragments random joining: NA |
| Download |
|
Study Data File |
| |
| Chromothripsis Cases |
| U1 |
| |
|
|
| |
Case ID: |
U1 |
| |
Chromosome: | 6 |
| |
Disease type: |
Acute lymphoblastic leukemia |
| |
Technology: |
SNP Array |
| |
Platform: |
Illumina Humancnv370-Duo BeadChip |
| |
Affected Gene: |
Gene List |
| |
Download: |
Copy Number File |
| |  |
|
