Variant DetailsVariant: esv2656893 Internal ID | 9576312 | Landmark | | Location Information | | Cytoband | 19p12 | Allele length | Assembly | Allele length | hg38 | 421 | hg19 | 421 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5969911, essv6067459, essv6309888, essv6316570, essv5891397, essv6577629, essv5851563, essv6339100, essv6389366, essv5799800, essv5764296, essv6471133, essv5930907, essv5737434, essv6212800, essv6014435, essv6243329, essv5931123, essv6425180, essv6230933, essv6092740, essv5626096, essv5570550, essv6043078, essv5641261 | Samples | HG00442, NA18621, HG01389, NA18530, NA19076, HG00589, HG01365, NA18964, NA18990, NA19657, HG01384, NA19663, HG00583, HG00404, HG01204, NA18546, HG00611, HG00319, HG00620, HG00614, HG01055, HG00310, HG00472, NA18622, NA18620 | Known Genes | ZNF93 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2656893
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 25 | Observed Complex | 0 | Frequency | n/a |
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