Variant DetailsVariant: esv2662377 Internal ID | 9581796 | Landmark | | Location Information | | Cytoband | 1p36.32 | Allele length | Assembly | Allele length | hg38 | 349 | hg19 | 349 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6429513, essv5512908, essv5987147, essv5752439, essv6538462, essv5642389, essv5990786, essv6032443, essv6461104, essv6337981, essv6189458, essv6172207, essv6129654, essv5943685, essv6373808, essv5774820, essv5781509, essv6504564, essv5543393, essv6521146, essv5555654, essv6506679, essv6224723, essv5806442, essv5977786, essv6112108, essv6201697, essv5703019, essv6588994, essv5730609, essv5926716, essv6191098, essv5841234, essv5678624, essv6422607, essv5850489, essv5659194, essv5545290, essv6181202, essv6508168, essv5649876, essv5848025, essv5647864, essv6230481, essv6322722, essv6249623, essv6091377, essv6251044, essv6356412, essv6292284, essv5840446, essv5744813, essv5783985, essv5779366, essv6542459, essv6526641, essv5904917, essv5874746, essv5710521, essv6306676, essv6068129, essv6448046, essv5462076, essv5930357, essv6157596, essv6163803, essv6116683, essv5731192, essv6584466, essv5431659, essv6125869, essv6027703, essv5983683, essv6337398, essv5755154, essv5875036, essv5542135, essv6252831, essv5861509, essv5812292, essv5675554, essv6091505, essv5541246, essv6298081, essv5675793, essv5397932, essv6020196, essv6015486, essv5926559, essv5464148, essv5896676, essv6244611, essv5529709, essv6117538, essv6153613, essv5848289, essv5478028, essv6082472, essv5494452, essv5443857, essv6025286, essv5526373, essv6100803, essv6568601, essv6274084, essv6225449, essv5651766, essv5398800, essv6391630, essv6387702, essv6000764, essv5665526, essv5501467, essv5424731, essv6245572, essv6049657, essv5899828, essv6395125, essv5828794, essv5559838, essv5693036, essv5406361, essv5771735, essv6089295, essv5665082, essv6286208, essv6193640 | Samples | HG01060, HG00650, HG00442, HG01462, NA18621, HG00249, HG01079, NA18599, HG01389, HG01374, HG00315, HG00151, HG00318, HG00699, NA18596, NA18530, NA12058, NA18606, HG00150, HG00337, HG01350, NA18519, HG00251, NA18597, HG01351, NA18595, HG00702, NA18635, NA18619, NA18558, HG00330, NA18574, HG00346, HG00369, HG01365, HG00334, HG00590, HG00277, HG01069, NA19720, HG01080, HG01067, HG01170, HG01072, HG00534, HG00422, HG00705, HG00309, HG00427, NA18990, HG00338, HG00159, HG00464, HG01124, HG00543, HG01183, HG01136, HG00154, NA18544, NA19657, HG00443, HG00557, HG00428, HG00653, HG00701, HG00436, HG00584, HG00533, HG00344, NA18637, HG01498, HG00500, NA18910, NA18534, HG00619, HG00708, NA18548, HG00324, HG01073, HG00651, HG00250, HG00690, HG00331, HG01101, HG00321, HG01334, HG00276, HG00463, NA18536, HG01107, HG01204, NA19436, NA18546, NA12043, HG00124, NA18542, NA19834, NA18543, NA18559, HG00580, HG00734, NA07051, HG01375, HG00607, HG00256, HG00620, HG00125, HG00707, HG00672, HG00111, HG00513, HG00478, HG00421, HG00656, HG00342, HG00123, NA20510, HG00310, NA07056, NA19312, HG01125, NA19463, NA18612, NA18549, HG00437, HG00581, NA18620 | Known Genes | PRDM16 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2662377
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 127 | Observed Complex | 0 | Frequency | n/a |
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