Variant DetailsVariant: esv2716535| Internal ID | 10300171 | | Landmark | | | Location Information | | | Cytoband | 17q25.3 | | Allele length | | Assembly | Allele length | | hg38 | 280 | | hg19 | 280 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | dgv440e201 | | Supporting Variants | essv6898174, essv6916837, essv6678566, essv6812747, essv6858343, essv6888584, essv6820536, essv6868067, essv6868068, essv6688878 | | Samples | SSM087, SSM096, SSM089, SSM035, SSM032, SSM078, SSM016, SSM076, SSM099 | | Known Genes | TBCD | | 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) | esv2716535
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 9 | | Observed Complex | 0 | | Frequency | n/a |
|
|