Variant DetailsVariant: esv2670257Internal ID | 9589676 | Landmark | | Location Information | | Cytoband | 5q33.1 | Allele length | Assembly | Allele length | hg38 | 4448 | hg19 | 4448 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5555148, essv6343442, essv6054239, essv5767210, essv5723370, essv5750755, essv6297194, essv6307929, essv5956480, essv5970127, essv6305204, essv6193902, essv6377042, essv6185129, essv5959095, essv5618952, essv6337010, essv6346108, essv6015461, essv6413426, essv5961005, essv6088693, essv6305882, essv5747371, essv6085760, essv6097772, essv5934020, essv6235692, essv6410661, essv6463237, essv6169649, essv6596357, essv5578316, essv6053317, essv6551861, essv5763199, essv5712488, essv6228831, essv6477855, essv6535352, essv5958095, essv6173784, essv6574994, essv5840763, essv6333332, essv6497059, essv5527355, essv5877358, essv6419067, essv5656513, essv5729685, essv5678135, essv6069359, essv6436358, essv5583356, essv5718940, essv5886067, essv6359292, essv6328253, essv6350903, essv6501651, essv5655997, essv6340994, essv5457921, essv5590751, essv5732390, essv6029350, essv5614749, essv6047885, essv5616228, essv5608253, essv5508298, essv5600943, essv5823446, essv5594757, essv5761616, essv5514841, essv6437965, essv6238695, essv5968291, essv6174293, essv5507413, essv6027484, essv5486759, essv5729865, essv5937595, essv5761016, essv5720172, essv6200420, essv6451889, essv6289434, essv5428375, essv5849159, essv6270064, essv5448883, essv5916982, essv5491788, essv6154309, essv5838221, essv6202021, essv6446981, essv5420350, essv5783488, essv6072853, essv6466334, essv5815201, essv5628974, essv5761598, essv6256463, essv6100723, essv6110471, essv6092151, essv5532023, essv6245904, essv5560564, essv5518880, essv5617315, essv5521472, essv5905333, essv5929565, essv6281418, essv5480167, essv6369897, essv6500192, essv6228334, essv6244130, essv5689718, essv5874694, essv5889125, essv5785968, essv6043472, essv5938152, essv5663398, essv5982626, essv6113187 | Samples | HG00542, HG00442, NA19058, NA19055, HG00608, NA18621, NA11829, HG00671, NA19066, NA18592, HG00559, HG00524, NA18565, NA18561, NA18599, NA12751, NA19057, NA18530, NA12058, NA18959, NA18526, NA12400, NA12399, NA19067, NA12341, NA12813, NA18967, NA18563, NA18940, HG00501, HG00702, NA18982, NA18547, HG00634, NA18942, NA11918, NA18582, NA19088, NA19054, NA18964, HG00537, NA19079, NA18949, HG00590, HG00512, NA12282, NA18977, NA11932, NA18560, HG00422, NA19087, HG00427, NA18985, NA18973, HG00530, HG00419, NA19007, NA18614, NA10847, HG00543, NA18951, NA18544, HG00629, HG00443, NA19056, HG00596, HG00557, HG00701, HG00475, HG00436, HG00583, NA18637, NA18572, HG00619, HG00708, NA18548, NA18566, NA18573, HG00651, NA19000, HG00690, HG00479, NA18532, HG00613, NA19059, NA18555, NA18963, HG00704, NA18536, NA18570, NA18593, NA12546, NA18541, NA19012, NA18576, NA18535, NA18564, NA18628, NA19072, NA18941, NA07051, NA19010, HG00473, HG00662, HG00418, NA12347, NA06986, HG00620, NA19078, HG00614, HG00478, NA18971, NA18631, HG00421, NA18987, HG00656, NA18636, NA12830, NA18609, HG00698, NA11843, NA18552, NA18983, NA18984, NA07056, NA18989, NA11892, NA12890, NA18623, NA19063, NA19065, NA19074, NA18622, NA12776, HG00593 | Known Genes | | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2670257
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 135 | Observed Complex | 0 | Frequency | n/a |
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