ChromothripsisDB: a curated database of chromothripsis
 
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PubMed ID   24553141 Publish Date   2014 Feb
Journal   Nature Species   Homo sapiens
Disease Type   Ependymoma Technology   Next Generation Sequencing
Case Number   9 Raw Data   EBI: EGAS00001000254
Title   C11orf95-RELA fusions drive oncogenic NF-kappaB signalling in ependymoma.
Authors   Parker M, Mohankumar KM, Punchihewa C, Weinlich R, Dalton JD, Li Y, Lee R, Tatevossian RG, Phoenix TN, Thiruvenkatam R, White E, Tang B, Orisme W, Gupta K, Rusch M, Chen X, Li Y, Nagahawhatte P, Hedlund E, Finkelstein D, Wu G, Shurtleff S, Easton J, Boggs
Affiliation   St. Jude Children's Research Hospital - Washington University Pediatric Cancer Genome Project, Memphis, Tennessee 38105, USA
Chromothripsis Definition   Close-by breakpoints: >=4
Copy number states: 2-3
Fragments random joining: Yes
Download   Study Data File
 
Chromothripsis Cases
  ST1
     
  Case ID: ST1
  Chromosome:11,X
  Disease type: Ependymoma
  Technology: Next Generation Sequencing
  Platform: Illumina HighSeq
  Affected Gene: Gene List
  Download: Copy Number File   Links File
  ST2
     
  Case ID: ST2
  Chromosome:1,11
  Disease type: Ependymoma
  Technology: Next Generation Sequencing
  Platform: Illumina HighSeq
  Affected Gene: Gene List
  Download: Copy Number File   Links File
  ST3
     
  Case ID: ST3
  Chromosome:11
  Disease type: Ependymoma
  Technology: Next Generation Sequencing
  Platform: Illumina HighSeq
  Affected Gene: Gene List
  Download: Copy Number File   Links File
  ST4
     
  Case ID: ST4
  Chromosome:2,11
  Disease type: Ependymoma
  Technology: Next Generation Sequencing
  Platform: Illumina HighSeq
  Affected Gene: Gene List
  Download: Copy Number File   Links File
  ST5
     
  Case ID: ST5
  Chromosome:6,8,11
  Disease type: Ependymoma
  Technology: Next Generation Sequencing
  Platform: Illumina HighSeq
  Affected Gene: Gene List
  Download: Copy Number File   Links File
  ST6
     
  Case ID: ST6
  Chromosome:11
  Disease type: Ependymoma
  Technology: Next Generation Sequencing
  Platform: Illumina HighSeq
  Affected Gene: Gene List
  Download: Copy Number File   Links File
  ST7
     
  Case ID: ST7
  Chromosome:6,11
  Disease type: Ependymoma
  Technology: Next Generation Sequencing
  Platform: Illumina HighSeq
  Affected Gene: Gene List
  Download: Copy Number File   Links File
  ST8
     
  Case ID: ST8
  Chromosome:11
  Disease type: Ependymoma
  Technology: Next Generation Sequencing
  Platform: Illumina HighSeq
  Affected Gene: Gene List
  Download: Copy Number File   Links File
  ST16
     
  Case ID: ST16
  Chromosome:4,11
  Disease type: Ependymoma
  Technology: Next Generation Sequencing
  Platform: Illumina HighSeq
  Affected Gene: Gene List
  Download: Copy Number File   Links File
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