Variant DetailsVariant: esv3637194![](http://dgv.tcag.ca/gb2/gbrowse_img/dgv2_hg38/?name=chr15:89416268..89418428;width=800;overview=1) Internal ID | 6677301 | Landmark | | Location Information | | Cytoband | 15q26.1 | Allele length | Assembly | Allele length | hg38 | 2161 | hg19 | 2161 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15317154, essv15317156, essv15317143, essv15317135, essv15317133, essv15317137, essv15317153, essv15317157, essv15317140, essv15317150, essv15317139, essv15317132, essv15317145, essv15317148, essv15317146, essv15317158, essv15317151, essv15317131, essv15317152, essv15317138, essv15317136, essv15317155, essv15317141, essv15317142, essv15317147, essv15317144, essv15317149, essv15317134 | Samples | HG01850, NA19020, HG01806, HG02058, HG02382, HG02356, NA19443, HG02023, HG02374, HG01840, HG02136, HG01841, HG00598, HG02522, HG02165, HG00692, HG02081, HG02184, NA18531, HG01596, NA18646, NA18628, HG02137, HG02128, HG02367, HG01804, HG01872, HG00978 | Known Genes | | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3637194
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 28 | Observed Complex | 0 | Frequency | n/a |
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