ChromothripsisDB: a curated database of chromothripsis
 
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PubMed ID   24143197 Publish Date   2013 Oct
Journal   PLoS One Species   Homo sapiens
Disease Type   Cri-du-chat syndrome Technology   Array CGH
Case Number   2 Raw Data  
Title   A Familial Cri-du-Chat/5p Deletion Syndrome Resulted from Rare Maternal Complex Chromosomal Rearrangements (CCRs) and/or Possible Chromosome 5p Chromothripsis
Authors   Heng Gu, Jian-hui Jiang, Jian-ying Li, Ya-nan Zhang, Xing-sheng Dong, Yang-yu Huang, Xinming Son, Xinyan Lu, Zheng Chen
Affiliation   Department of Medical Genetics, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, PR China
Chromothripsis Definition   Close-by breakpoints: >=6
Copy number states: 2
Fragments random joining: NA
Download   Study Data File
 
Chromothripsis Cases
  mother
     
  Case ID: mother
  Chromosome:5
  Disease type: Cri-du-chat syndrome
  Technology: Array CGH
  Platform: Agilent 4x180K array
  Affected Gene: Gene List
  daughter
     
  Case ID: daughter
  Chromosome:5
  Disease type: Cri-du-chat syndrome
  Technology: Array CGH
  Platform: Agilent 4x180K array
  Affected Gene: Gene List
 
© 2015 Cai Laboratory.  Last updated on 13 Mar 2018