Variant DetailsVariant: esv2671430 | Internal ID | 9937535 | | Landmark | | | Location Information | | | Cytoband | 15q23 | | Allele length | | Assembly | Allele length | | hg38 | 1023 | | hg19 | 1023 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6182400, essv5397052, essv6197666, essv5888651, essv5664949, essv5803773, essv5939562, essv5613711, essv6224134, essv5994987, essv6250750, essv6339310, essv6485165, essv6461646, essv6150544, essv5454895, essv5835636, essv6054782, essv6478404, essv6234189, essv6373526, essv5555423, essv5785435, essv5726092, essv6593007, essv5534709, essv5900878, essv5933748, essv5501870, essv6354816, essv5405459, essv6410886, essv6097650, essv5717594, essv5664941, essv5438861, essv6242069, essv6354353, essv6419757, essv6299977, essv6330256, essv5489883, essv6309132, essv5853491, essv5665461, essv5538246, essv5404672, essv6471813, essv5491589, essv5474123, essv5756649, essv5463853, essv5855946, essv6396532, essv6173227, essv6246260, essv6097065, essv5513336, essv5580315, essv5748389, essv6193124, essv6430823, essv5865871, essv6161115, essv6479714, essv5618993, essv6476390, essv5894119, essv6036533, essv6197254, essv5532424, essv5629412, essv6533995, essv6074070, essv5524107, essv5623766, essv5556536, essv5869383, essv6178900, essv6178545, essv6522270, essv5893078, essv6509332, essv6177244, essv5449090, essv5675709 | | Samples | HG00249, HG00671, HG00187, NA18565, HG01389, HG00315, NA20813, HG00367, NA18606, HG00449, HG01461, HG00261, NA18988, NA12341, HG00271, HG01350, HG00501, HG00448, NA18558, NA18547, NA18574, HG00346, HG00247, NA19720, NA19651, HG01072, NA19471, HG01440, HG00427, HG00118, NA19189, HG00326, HG00323, NA18638, HG01353, HG00543, HG00313, HG01136, NA18544, HG00560, HG00183, HG01187, NA19070, HG00557, HG00328, HG00428, NA19462, HG00701, HG00533, HG00583, NA18637, NA12718, NA18534, HG00651, HG00684, HG00704, HG00463, NA19469, NA18536, NA18546, NA18632, HG00476, NA18543, NA19434, HG00366, NA18628, NA19072, NA18950, HG00580, HG00357, HG00638, HG00278, HG00607, HG00256, NA19085, HG00513, HG00259, NA19472, HG00421, HG00174, HG00280, HG00343, HG00472, NA19004, HG00180, HG00581 | | Known Genes | MAP2K5 | | Method | Merging | | Analysis | No reference, merging analysis | | Platform | Merging | | Comments | High quality site | | Reference | 1000_Genomes_Consortium_Phase_1 | | Pubmed ID | 23128226 | | Accession Number(s) | esv2671430
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 86 | | Observed Complex | 0 | | Frequency | n/a |
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