Variant DetailsVariant: esv2665506 Internal ID | 9584925 | Landmark | | Location Information | | Cytoband | 19p13.13 | Allele length | Assembly | Allele length | hg38 | 848 | hg19 | 848 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6143623, essv6305111, essv6554284, essv5518865, essv5552302, essv5643663, essv5992829, essv6058329, essv5989351, essv5399181, essv6447530, essv6423668, essv5890167, essv6016983, essv6123436, essv6462166, essv6457803, essv6289303, essv6201357, essv6387830, essv6518991, essv5685392, essv5831397, essv6529660, essv5671284, essv5964959, essv5433041, essv6165651, essv6449298, essv5451423, essv5474591, essv5908180, essv6234267, essv5763527, essv5942540, essv6167180, essv6385936, essv6315454, essv6383223, essv5430592, essv5590656, essv6578905, essv6500188, essv6520927, essv5408113, essv6236340, essv5965001, essv5783549, essv5471930, essv5851907 | Samples | HG00734, HG01072, HG01052, HG01075, HG01055, HG01173, HG01083, HG00731, HG01098, HG01079, HG01197, HG01051, HG01082, HG01174, HG00553, HG01182, HG01167, HG01188, HG01204, HG01101, HG01168, HG00737, HG01171, HG00554, HG01107, HG01048, HG01061, HG01183, HG01047, HG01187, HG01097, HG01191, HG00640, HG01066, HG00732, HG01073, HG01170, HG01069, HG01176, HG01080, HG00740, HG01070, HG01060, HG01190, HG01095, HG01108, HG00641, HG01102, HG01067, HG01198 | Known Genes | ZSWIM4 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2665506
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 50 | Observed Complex | 0 | Frequency | n/a |
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