Variant DetailsVariant: esv2668886 Internal ID | 9588305 | Landmark | | Location Information | | Cytoband | 7q11.22 | Allele length | Assembly | Allele length | hg38 | 178 | hg19 | 178 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6343741, essv6137399, essv6237529, essv5553337, essv6310544, essv5795938, essv5705868, essv5831117, essv6129646, essv6043930, essv5947501, essv6224837, essv6408832, essv6071970, essv6461847, essv5985801, essv6021446, essv6471495, essv6101149, essv6281287, essv6056381, essv6260931, essv5971349, essv5856638, essv5536528, essv6498658, essv6171731, essv5765068, essv6598103, essv6164361, essv5750480, essv5615745, essv5929954, essv5580754, essv5989698, essv6197079, essv6047709, essv6588845, essv5490415, essv5673656, essv5856464, essv6384907, essv5943527, essv5602350, essv6331421 | Samples | HG01060, HG01173, NA19703, HG01389, HG01066, HG00315, NA19377, HG00261, HG00271, HG01350, HG01492, HG01354, HG00139, HG00277, HG00335, HG01072, HG00232, HG00427, HG01048, HG00253, HG00108, HG00137, HG00154, NA18613, HG00443, NA19707, HG00428, HG00701, HG00344, NA18910, HG01073, HG00250, HG01383, HG00246, HG00126, HG00375, HG00136, HG01375, NA06986, HG00125, HG00707, HG00329, HG00123, HG00310, HG01082 | Known Genes | WBSCR17 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2668886
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 45 | Observed Complex | 0 | Frequency | n/a |
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