Variant DetailsVariant: dgv1332e201Internal ID | 20126219 | Landmark | | Location Information | | Cytoband | Yq11.21 | Allele length | Assembly | Allele length | hg38 | 1003 | hg19 | 1003 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv2740655, esv2740659, esv2740663 | Samples | SSM008, SSM027, SSM024, SSM084, SSM090, SSM018, SSM096, SSM017, SSM003, SSM067, SSM085, SSM082, SSM016, SSM037, SSM055 | Known Genes | | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | dgv1332e201
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 15 | Observed Complex | 0 | Frequency | n/a |
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