Variant DetailsVariant: esv2659026 Internal ID | 9578445 | Landmark | | Location Information | | Cytoband | 7p15.1 | Allele length | Assembly | Allele length | hg38 | 844 | hg19 | 844 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1189e199 | Supporting Variants | essv6045507, essv6506101, essv6243011, essv5532999, essv5722341, essv6319866, essv5839266, essv5632281, essv5721602, essv6075541, essv5608389, essv6462987, essv5470058, essv6240518, essv6343329, essv6596370, essv5913070, essv5689924, essv6104249, essv6469808, essv5584417, essv6079408, essv6545099, essv6149881, essv6369710, essv5460061, essv6518309, essv5886942, essv6472032, essv5490490, essv5714610, essv6094305, essv5595184, essv5936775, essv5660487, essv6542943, essv6559407, essv6338274, essv6194510, essv5483577, essv6176823, essv5777854, essv6314992, essv6568572, essv5757110, essv5824229, essv6571722, essv5837679, essv6524464, essv6217623, essv6585850, essv5499908, essv6495258, essv5426144, essv6415626, essv5497674, essv6099985, essv5463291, essv6420046, essv5795743, essv5723821, essv6333661, essv5940011, essv5765020, essv6518799, essv6017367, essv5594033, essv6134875, essv6017489, essv5761569, essv6522780, essv5685824, essv5917052, essv6110036, essv6040374, essv6167444, essv6328648, essv5535990, essv6432084, essv6089289, essv6187589, essv5705185, essv6019735 | Samples | HG00096, HG01060, HG00114, HG01441, HG01173, HG01098, HG00249, HG00242, HG00100, HG01188, HG01066, HG00233, HG01465, HG00103, HG01456, HG00115, HG00150, HG01051, HG00261, HG01140, HG00127, HG01366, HG01488, HG01167, HG00736, HG01083, HG00247, HG01365, HG00243, HG00158, HG01134, HG00139, HG01069, HG01067, HG00120, HG00148, HG00106, HG00236, HG00262, HG01072, HG01440, HG01198, HG00159, HG01048, HG00108, HG00133, HG01183, HG01136, HG00154, HG00731, HG00245, HG00732, HG01498, HG01149, HG01390, HG01383, HG00117, HG01101, HG00157, HG00152, HG00246, HG01107, HG01204, HG01148, HG00258, HG00124, HG00119, HG01190, HG00734, HG00136, HG00638, HG01137, HG00116, HG00111, HG00259, HG00123, HG00112, HG00252, HG01082, HG01125, HG01112, HG00554, HG01061 | Known Genes | CREB5 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2659026
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 83 | Observed Complex | 0 | Frequency | n/a |
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