Variant DetailsVariant: esv2672889 Internal ID | 9592308 | Landmark | | Location Information | | Cytoband | 16q24.2 | Allele length | Assembly | Allele length | hg38 | 238 | hg19 | 238 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5418185, essv6284095, essv5739735, essv6346905, essv6418363, essv5966623, essv5484842, essv6325623, essv6454995, essv6370679, essv6016524, essv6141475, essv6379710, essv5489506, essv5960978, essv6378691, essv5639719, essv6509392, essv5758382, essv6113232, essv6095658, essv5506920, essv5516812, essv5863698, essv5543003, essv6478905, essv6282769, essv6157717, essv6566754, essv5673064, essv5535317, essv5512280, essv6451813, essv5699898, essv5806099, essv5775247, essv5495888, essv5423077, essv5962690, essv6550393, essv6068659, essv5919092, essv6337456, essv6216914, essv6224591, essv6162919, essv5405131, essv5732341, essv5828890, essv5717111, essv6003638, essv5519936, essv6247312, essv5847577, essv6544651, essv5758573, essv5541886, essv6220705, essv5796960, essv5484309, essv6391451, essv5452917, essv6130330, essv5561217, essv5925232, essv5561058, essv6098782, essv5406257, essv6148594, essv6440176, essv5729831, essv5824299, essv6102795, essv6511789, essv5901702, essv5890041, essv5941301, essv6208456, essv5730047, essv5490550, essv5999201, essv6146607, essv5722863, essv6136303, essv6533532, essv5855606, essv5525723, essv5944801, essv5921470, essv5540788, essv5837359, essv5769760, essv6029936, essv6006938, essv5540527, essv6058202 | Samples | NA18621, HG00537, HG01440, NA18534, HG01353, NA18530, NA19819, HG01055, HG00705, HG00500, HG01173, NA18612, HG00464, HG00131, HG00707, HG00463, HG00657, HG00614, HG01365, HG00475, HG00542, HG01174, NA18546, HG00701, HG00683, HG01188, HG00581, HG00280, HG01101, HG00319, NA18557, HG01171, NA18596, HG00342, HG00543, HG01107, NA18559, HG01375, HG00421, HG00583, NA18635, NA18536, HG01048, HG00692, HG01047, NA18636, HG00315, HG00533, HG00419, HG00125, NA18637, HG01187, HG00237, HG00584, HG00662, HG00620, HG01437, NA18633, HG00653, HG01066, NA18558, HG00501, HG00672, HG00478, HG01351, HG00740, NA18613, HG00513, HG00524, HG00512, HG00534, HG00246, HG00589, NA18606, NA18543, HG00427, HG00443, NA18599, HG00650, HG00448, NA18602, HG00608, HG01390, HG00422, HG01108, HG00693, NA18611, NA18549, HG00442, HG00684, HG00476, HG00704, HG00271, HG00531, HG01067, HG00327 | Known Genes | BANP | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2672889
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 96 | Observed Complex | 0 | Frequency | n/a |
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