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 | essv5560972, essv6581508, essv6163309, essv6172346, essv5976704, essv6391905, essv6237872, essv6347124, essv6399654, essv6170762, essv6553283, essv5616026, essv6211840, essv6432190, essv5733986, essv6429804, essv6070811, essv5554355, essv6185616, essv5748997, essv5501854, essv5492070, essv6456073, essv5942978, essv6376233, essv5508181, essv6037415, essv6029513, essv5535021, essv5942484, essv5731798, essv5757318, essv5615371, essv6539045, essv5435502, essv5887077, essv5480374, essv6254168, essv6529818, essv5913647, essv6592608, essv6445474, essv6272957, essv5486867, essv6531462, essv5822633, essv6378652, essv5506514, essv5600096, essv6495014, essv6485296, essv6331761, essv6226112, essv5505966, essv6015808, essv5849491, essv6073585, essv6098361, essv5442519, essv5549413, essv5681090, essv5770819, essv6269753, essv6041105, essv6266415, essv5888355, essv6440450, essv5686556, essv6356329, essv5997831, essv6441325, essv6104856, essv5630155, essv6162611, essv6090282, essv6283788, essv5489926, essv6558083, essv6236451, essv5472976, essv6447619, essv5598130, essv5470521, essv6184608, essv6541244, essv5742708, essv6078494, essv6470698, essv6170584, essv5705454, essv6020381, essv6008461, essv5994947, essv5545656, essv6230556, essv6348630, essv6271142, essv5928512, essv6265847, essv5821118, essv5575755, essv5734787, essv5499292, essv6420824, essv5900336, essv5844004, essv6451608, essv5848973, essv6557558, essv5401585, essv6238456, essv6323092, essv6095960, essv5493845, essv6423442, essv6185001, essv6144134, essv6085684, essv5729573, essv6018923, essv6115715, essv6070511, essv5949369, essv6316077, essv6081381, essv6146744, essv6205111, essv6547351 | | Samples | HG00323, HG00613, NA12718, HG00152, HG00607, NA18616, NA20771, NA11930, HG00619, NA18534, HG00344, NA18530, NA18535, HG01052, HG00705, HG00437, HG00500, HG01173, NA18612, NA20796, NA18526, HG00449, NA18570, NA19003, HG00463, HG00614, HG00577, HG00428, HG00475, HG00148, NA20786, HG00553, HG00139, NA18541, HG00683, HG00698, HG00651, HG00699, NA18950, HG00479, NA18596, NA18632, HG00244, HG00543, HG00154, NA19062, HG00321, HG00556, NA18627, NA19059, NA19076, HG00421, HG00583, NA20811, NA18622, NA18960, HG01048, NA18990, HG00689, NA18636, NA18592, NA07048, NA18547, NA12400, NA18637, HG00174, NA18982, HG00254, HG00276, HG00237, HG00662, NA20769, HG00436, HG00620, HG00653, NA18572, HG00629, HG00559, NA19657, HG00560, HG00265, HG00672, NA20814, NA19909, NA18613, HG00513, HG00524, NA20582, HG00512, HG00534, HG00525, NA19074, HG00377, NA19789, HG00589, NA18606, HG00120, NA18940, NA12890, NA18582, HG00427, NA18597, HG00590, NA18599, HG00663, HG00262, NA18560, NA18544, HG00608, NA18577, HG00654, HG00656, HG00422, NA18610, NA19070, NA18984, HG00690, HG00473, HG00684, NA20502, NA19087, HG00702, HG00704, HG00278, HG00136, NA12775, NA19058, HG00531 | | 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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