| PubMed ID |
|
23271725 |
Publish Date |
|
2013 Mar |
| Journal |
|
Cancer Res |
Species |
|
Homo sapiens |
| Disease Type |
|
Melanoma |
Technology |
|
Array CGH |
| Case Number |
|
2 |
Raw Data |
|
|
| Title |
|
Chromothripsis and Focal Copy Number Alterations Determine Poor Outcome in Malignant Melanoma |
| Authors |
|
Hirsch D, Kemmerling R, Davis S, Camps J, Meltzer PS, Ried T, Gaiser T |
| Affiliation |
|
Genetics Branch, Center for Cancer Research, National Cancer Institute/NIH, Bethesda, Maryland 20892, USA |
| Chromothripsis Definition |
|
Close-by breakpoints: >=12
Copy number states: 2-3
Fragments random joining: NA |
| Download |
|
Study Data File |
| |
| Chromothripsis Cases |
| case14 |
| |
|
|
| |
Case ID: |
case14 |
| |
Chromosome: | 5,20 |
| |
Disease type: |
Melanoma |
| |
Technology: |
Next Generation Sequencing |
| |
Platform: |
Illumina HiSeq 2000 |
| | | case20 |
| |
|
|
| |
Case ID: |
case20 |
| |
Chromosome: | 5,15 |
| |
Disease type: |
Melanoma |
| |
Technology: |
Array CGH |
| |
Platform: |
Agilent CGH Microarrays 4x180 K |
| |
|
