| PubMed ID |
|
26856307 |
Publish Date |
|
2016 Jun |
| Journal |
|
Int J Cancer |
Species |
|
Homo sapiens |
| Disease Type |
|
Li-Fraumeni syndrome |
Technology |
|
Next Generation Sequencing |
| Case Number |
|
4 |
Raw Data |
|
|
| Title |
|
Telomere dysfunction and chromothripsis |
| Authors |
|
Ernst A, Jones DT, Maass KK, Rode A, Deeg KI, Jebaraj BM, Korshunov A, Hovestadt V, Tainsky MA, Pajtler KW, Bender S, Brabetz S, Grobner S, Kool M, Devens F, Edelmann J, Zhang C, Castelo-Branco P, Tabori U, Malkin D, Rippe K, Stilgenbauer S, Pfister SM, Zapatka M, Lichter P |
| Affiliation |
|
Division of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany |
| Chromothripsis Definition |
|
Close-by breakpoints: >8
Copy number states: 2--4
Fragments random joining: No |
| Download |
|
Study Data File |
| |
| Chromothripsis Cases |
| LFS MDAH087 p145 |
| |
|
|
| |
Case ID: |
LFS MDAH087 p145 |
| |
Chromosome: | 15 |
| |
Disease type: |
Li-Fraumeni syndrome |
| |
Technology: |
Next Generation Sequencing |
| |
Platform: |
Illumina MiSeq |
| | | LFS MDAH172 p170 |
| |
|
|
| |
Case ID: |
LFS MDAH172 p170 |
| |
Chromosome: | 8 |
| |
Disease type: |
Li-Fraumeni syndrome |
| |
Technology: |
Next Generation Sequencing |
| |
Platform: |
Illumina MiSeq |
| | | LFS MDAH174 p84 |
| |
|
|
| |
Case ID: |
LFS MDAH174 p84 |
| |
Chromosome: | 1 |
| |
Disease type: |
Li-Fraumeni syndrome |
| |
Technology: |
Next Generation Sequencing |
| |
Platform: |
Illumina MiSeq |
| | | LFS MDAH041 p308 |
| |
|
|
| |
Case ID: |
LFS MDAH041 p308 |
| |
Chromosome: | 15 |
| |
Disease type: |
Li-Fraumeni syndrome |
| |
Technology: |
Next Generation Sequencing |
| |
Platform: |
Illumina MiSeq |
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