PubMed ID |
|
25625332 |
Publish Date |
|
2015 Jan |
Journal |
|
Nature Communications |
Species |
|
Homo sapiens |
Disease Type |
|
Pheochromocytomas and paragangliomas |
Technology |
|
SNP Array |
Case Number |
|
3 |
Raw Data |
|
|
Title |
|
Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas |
Authors |
|
Castro-Vega LJ, Letouze E, Burnichon N, Buffet A, Disderot PH, Khalifa E, Loriot C, Elarouci N, Morin A, Menara M, Lepoutre-Lussey C, Badoual C, Sibony M, Dousset B, Libe R, Zinzindohoue F, Plouin PF, Bertherat J, Amar L, de Reynies A, Favier J, Gimenez-Roqueplo AP |
Affiliation |
|
INSERM, UMR970, Paris-Cardiovascular Research Center, F-75015 Paris, France |
Chromothripsis Definition |
|
Close-by breakpoints: >=10 Copy number states: 3-4 Fragments random joining: NA |
Download |
|
Study Data File |
|
Chromothripsis Cases |
37 |
|
|
|
|
Case ID: |
37 |
|
Chromosome: | 1,5,17 |
|
Disease type: |
Pheochromocytomas and paragangliomas |
|
Technology: |
SNP Array |
|
Platform: |
Illumina HumanCNV610-Quad v1.0. Hybridization |
| | 49 |
|
|
|
|
Case ID: |
49 |
|
Chromosome: | 1,5,17 |
|
Disease type: |
Pheochromocytomas and paragangliomas |
|
Technology: |
SNP Array |
|
Platform: |
Illumina HumanCNV610-Quad v1.0. Hybridization |
| | 188 |
|
|
|
|
Case ID: |
188 |
|
Chromosome: | 1,5,17 |
|
Disease type: |
Pheochromocytomas and paragangliomas |
|
Technology: |
SNP Array |
|
Platform: |
Illumina HumanCNV610-Quad v1.0. Hybridization |
| |
|