Variant DetailsVariant: esv2660901 Internal ID | 9580320 | Landmark | | Location Information | | Cytoband | 17q23.2 | Allele length | Assembly | Allele length | hg38 | 2025 | hg19 | 2025 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv559e199 | Supporting Variants | essv5928588, essv5709345, essv5403538, essv5620591, essv6302877, essv5903531, essv5731464, essv6583778, essv5447871, essv5489474, essv6021852, essv5657552, essv6542425, essv5850042, essv5664068, essv6537964, essv5510351, essv5454064, essv6372031, essv6155227, essv5848505, essv5843174, essv6185274, essv5985200, essv5616644, essv5953275, essv5634420, essv6367705, essv6183733, essv5437851, essv6324861, essv6496986, essv6257406, essv6412797, essv6568608, essv6249069, essv5466030, essv5941014, essv6052844, essv5896836, essv6512186, essv5567593, essv6070237, essv5905720, essv5481898, essv5466549, essv6144531, essv5734847, essv6098672, essv5409738, essv6348208, essv6520576, essv5853048, essv5557986, essv5997411, essv6321159, essv6222645, essv5766948, essv5568551, essv5436388, essv5761534, essv6542278, essv5505450, essv6439738, essv5540314, essv6386762, essv6193603, essv6034976, essv6297223, essv5453813, essv6526315, essv5658042, essv5547426, essv6138085, essv6218423, essv6289872, essv6182283, essv6231953, essv6236046, essv5947400, essv6087367, essv6584913, essv6157462, essv5943024, essv6318722, essv6517666, essv6559435, essv6143747, essv6188911, essv5647220, essv6578440, essv6163273, essv5751038, essv6253715, essv5873069, essv6179376, essv5526757, essv6436637, essv5527484, essv6387074, essv5473160, essv6415862, essv6366672, essv6201097, essv5664330, essv6074096, essv5715724, essv6078101, essv6430157, essv6477413, essv5835462, essv6356855, essv6008547, essv5438188, essv5405095, essv5741054 | Samples | HG01441, NA19397, NA18924, HG01462, NA19909, NA20508, NA19466, NA19332, NA19704, HG00315, NA19359, HG01465, NA19355, NA19819, NA19057, NA19684, HG00737, NA20346, NA20507, HG01051, HG01140, HG00337, NA19107, NA19374, HG00641, NA19396, NA19381, NA19373, HG01488, NA18923, NA19457, HG01083, HG00247, HG00369, HG01365, NA19681, NA20291, NA19130, HG01134, NA18874, NA20340, NA19235, NA19471, NA19317, HG01198, HG00637, HG01048, NA19445, NA18867, HG00530, NA19921, NA19247, HG00176, NA19462, NA19347, NA20809, HG01095, NA19455, HG00584, HG01149, HG00692, HG01390, HG01047, NA19461, NA19449, NA19655, NA19453, NA18963, NA18523, NA19469, NA19625, NA19436, NA18576, NA19401, NA19375, NA18632, NA19652, NA19440, NA19390, HG00265, NA19834, NA19434, NA19473, NA19072, NA19435, NA18941, HG01375, NA19835, NA19439, NA19470, NA19311, HG01108, NA19360, NA20341, NA19818, NA19376, NA19398, NA19472, NA19223, NA19713, NA19213, NA19900, NA19430, HG01082, NA19316, HG00628, NA20322, NA18624, NA19463, HG01097, NA18612, NA19429, NA18487, HG00553, NA19431, NA18620 | Known Genes | USP32 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2660901
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 116 | Observed Complex | 0 | Frequency | n/a |
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