PubMed ID |
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29073611 |
Publish Date |
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2017 Oct |
Journal |
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Cytogenet Genome Res. |
Species |
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Homo sapiens |
Disease Type |
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Recurrent pregnancy loss |
Technology |
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Next Generation Sequencing |
Case Number |
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6 |
Raw Data |
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Title |
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Genomic Characterization of Chromosomal Insertions: Insights into the Mechanisms Underlying Chromothripsis |
Authors |
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Kato T, Ouchi Y, Inagaki H, Makita Y, Mizuno S, Kajita M, Ikeda T, Takeuchi K, Kurahashi H |
Affiliation |
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Division of Molecular Genetics, Institute for Comprehensive Medical Science (ICMS), Fujita Health University, Toyoake, Japan |
Chromothripsis Definition |
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Close-by breakpoints: 6 Copy number states: >=2 Fragments random joining: Yes |
Download |
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Study Data File |
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Chromothripsis Cases |
case_1 |
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Case ID: |
case_1 |
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Chromosome: | 4,14 |
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Disease type: |
Developmental delay |
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Technology: |
Next Generation Sequencing |
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Platform: |
Illumina HiSeq 1500 |
|
Download: |
Copy Number File |
| | | case_3 |
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|
|
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Case ID: |
case_3 |
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Chromosome: | 8,10,12 |
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Disease type: |
Langer-Giedion syndrome |
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Technology: |
Next Generation Sequencing |
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Platform: |
Illumina HiSeq 1500 |
|
Download: |
Copy Number File |
| | | case_4 |
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Case ID: |
case_4 |
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Chromosome: | 7 |
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Disease type: |
Recurrent pregnancy loss |
|
Technology: |
Next Generation Sequencing |
|
Platform: |
Illumina HiSeq 1500 |
|
Download: |
Copy Number File |
| | | case_1 |
|
|
|
|
Case ID: |
case_1 |
|
Chromosome: | 4,14 |
|
Disease type: |
Developmental delay |
|
Technology: |
Next Generation Sequencing |
|
Platform: |
Illumina HiSeq 1500 |
|
Download: |
Copy Number File |
| | | case_3 |
|
|
|
|
Case ID: |
case_3 |
|
Chromosome: | 8,10,12 |
|
Disease type: |
Langer-Giedion syndrome |
|
Technology: |
Next Generation Sequencing |
|
Platform: |
Illumina HiSeq 1500 |
|
Download: |
Copy Number File |
| | | case_4 |
|
|
|
|
Case ID: |
case_4 |
|
Chromosome: | 7 |
|
Disease type: |
Recurrent pregnancy loss |
|
Technology: |
Next Generation Sequencing |
|
Platform: |
Illumina HiSeq 1500 |
|
Download: |
Copy Number File |
| | | top |
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