ChromothripsisDB: a curated database of chromothripsis
 
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  Study
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
 
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