Variant DetailsVariant: esv2672879Internal ID | 9592298 | Landmark | | Location Information | | Cytoband | 15q25.2 | Allele length | Assembly | Allele length | hg38 | 1004687 | hg19 | 879166 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5935433, essv6354851 | Samples | HG01383, NA19390 | Known Genes | ALPK3, DNM1P41, GOLGA6L4, GOLGA6L5P, LINC00933, LOC388152, LOC440300, LOC642423, NMB, PDE8A, SCAND2P, SEC11A, SLC28A1, UBE2Q2P1, WDR73, ZNF592, ZSCAN2 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2672879
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
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