Variant DetailsVariant: esv2665192 | Internal ID | 9584611 | | Landmark | | | Location Information | | | Cytoband | 16q24.3 | | Allele length | | Assembly | Allele length | | hg38 | 1364 | | hg19 | 1364 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6205111, essv5630155, essv6447619, essv5486867, essv6376233, essv6265847, essv6172346, essv5549413, essv6399654, essv5928512, essv5600096, essv5435502, essv6541244, essv5545656, essv6378652, essv5770819, essv6018923, essv5844004, essv6391905, essv5598130, essv6237872, essv6041105, essv6553283, essv6095960, essv5734787, essv5757318, essv6495014, essv5472976, essv6558083, essv6008461, essv6070811, essv6085684, essv5493845, essv6090282, essv6441325, essv6098361, essv5731798, essv6531462, essv6323092, essv5849491, essv6470698, essv6185616, essv6429804, essv6451608, essv6015808, essv6104856, essv6592608, essv6283788, essv5401585, essv5821118, essv5994947, essv5615371, essv6269753, essv5887077, essv5748997, essv5900336, essv6078494, essv6557558, essv6271142, essv5997831, essv5480374, essv6547351, essv5501854, essv5942978, essv5505966, essv5616026, essv6238456, essv6146744, essv5705454, essv5470521, essv6529818, essv6347124, essv6348630, essv6266415, essv5508181, essv6230556, essv6081381, essv6445474, essv6456073, essv5560972, essv5888355, essv5822633, essv6073585, essv5729573, essv5554355, essv6316077, essv6423442, essv5681090, essv5742708, essv5575755, essv6420824, essv6485296, essv5489926, essv6185001, essv6070511, essv5686556, essv6236451, essv6356329, essv6029513, essv6163309, essv6272957, essv6184608, essv6440450, essv5442519, essv6162611, essv6144134, essv5848973, essv6432190, essv5913647, essv5535021, essv5499292, essv6254168, essv6170762, essv5942484, essv5976704, essv6581508, essv6115715, essv6539045, essv6226112, essv6170584, essv5949369, essv5492070, essv6020381, essv5733986, essv6331761, essv6211840, essv5506514, essv6037415 | | Samples | HG01173, NA19058, HG00608, NA19909, NA18592, HG00559, HG00524, HG01052, NA18599, HG00244, HG00699, NA18596, NA18530, NA18606, NA18616, HG00449, HG00654, NA18526, NA12400, NA20771, NA18627, HG00663, NA20814, NA19076, NA20796, NA18940, HG00589, NA18597, HG00702, HG00689, NA18982, NA20769, NA18547, NA18960, NA19062, NA07048, NA18582, HG00590, NA11930, HG00512, HG00139, HG00120, HG00683, HG00148, HG00262, NA18560, HG00534, HG00422, HG00705, NA19087, HG00427, NA20811, NA18990, HG01048, HG00323, NA19789, HG00543, HG00154, NA18544, HG00560, NA18613, HG00629, NA19657, NA19070, HG00428, HG00653, HG00577, HG00475, HG00436, HG00556, HG00583, HG00344, NA18637, HG00500, NA12718, NA18572, NA18534, HG00619, HG00651, HG00690, HG00531, HG00479, HG00684, HG00613, HG00525, HG00321, NA19059, HG00276, HG00152, HG00704, HG00463, NA18570, NA18541, NA19003, NA18632, HG00254, NA18535, HG00265, NA12775, NA18950, HG00136, HG00278, HG00473, HG00607, HG00237, HG00662, NA18610, HG00620, HG00672, HG00614, HG00513, NA20582, HG00421, HG00656, HG00174, NA18636, NA20786, HG00698, HG00377, NA20502, NA18984, NA12890, NA18612, NA19074, NA18622, HG00553, HG00437, NA18577 | | Known Genes | TCF25 | | Method | Merging | | Analysis | No reference, merging analysis | | Platform | Merging | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_1 | | Pubmed ID | 23128226 | | Accession Number(s) | esv2665192
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 128 | | Observed Complex | 0 | | Frequency | n/a |
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