ChromothripsisDB: a curated database of chromothripsis
 
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PubMed ID   25736334 Publish Date   2015 Apr
Journal   Am J Med Genet A Species   Homo sapiens
Disease Type   Dysmorphia Technology   Array CGH
Case Number   1 Raw Data  
Title   Constitutional chromothripsis involving chromosome 19 in a child with subtle dysmorphic features.
Authors   Wang JC, Fisker T, Sahoo T
Affiliation   Cytogenetics Laboratory, Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Ontario, Canada
Chromothripsis Definition   Close-by breakpoints: >=10
Copy number states: 3
Fragments random joining: NA
Download   Study Data File
 
Chromothripsis Cases
  25736334_1
     
  Case ID: 25736334_1
  Chromosome:19
  Disease type: Dysmorphia
  Technology: Array CGH
  Platform: 4x180 k oligonucleotide array
 
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