Variant DetailsVariant: esv2715148Internal ID | 9949434 | Landmark | | Location Information | | Cytoband | 16q24.3 | Allele length | Assembly | Allele length | hg38 | 278 | hg19 | 278 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6732760, essv6725102, essv6867908, essv6696203, essv6763752, essv6877134, essv6758622 | Samples | SSM092, SSM089, SSM045, SSM062, SSM047, SSM037, SSM059 | Known Genes | ANKRD11 | 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) | esv2715148
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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