Variant DetailsVariant: esv2669733 | Internal ID | 9935838 | | Landmark | | | Location Information | | | Cytoband | 8q24.22 | | Allele length | | Assembly | Allele length | | hg38 | 3048 | | hg19 | 3048 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6453509, essv5448016, essv5832216, essv6316464, essv5574522, essv5616055, essv5627283, essv5568719, essv5421443, essv5757889, essv6279424, essv6030540, essv6223877, essv6195533, essv5416485, essv6446755, essv6218328, essv6101728, essv6467130, essv5763631, essv6529369, essv6201223, essv6169698, essv6239542, essv5829158, essv6250316, essv5409482, essv5972434, essv5843957, essv6366546, essv5774033, essv5643925, essv6301747, essv5409789, essv5648283, essv5995308, essv6174057, essv5564576, essv5477129, essv6446577, essv5898953, essv5917823, essv5670978, essv5593108, essv5462623, essv5682889, essv5784908, essv6021600, essv6577118, essv6503081, essv6309894, essv6370830, essv5802134, essv5916852, essv6513160, essv6104935, essv5895247, essv5948082, essv5563730, essv5761672, essv5829068, essv6402595, essv6198276, essv6559027, essv6018247, essv6561919, essv5889905, essv5666084, essv5432718, essv6216382, essv5398415, essv5530857, essv6383197, essv6396287, essv6180130, essv6161988, essv6299165, essv6263512, essv6489532, essv5509210, essv6533804, essv5640434, essv5763585, essv6279163, essv5551812, essv6251264, essv6536636, essv6274232, essv6102800, essv6197311, essv6032548, essv6057581, essv5693170, essv6558734, essv6590198, essv5546926, essv5465359, essv5775369, essv6066203, essv5947747, essv6570886, essv5872108, essv5525138, essv6180285, essv5745869, essv6424795, essv5596547, essv6170140, essv6158342, essv6207799, essv6236305, essv6282076, essv6256228, essv5913003, essv6409727, essv6167898, essv5991805, essv5947327, essv5736678, essv5419728, essv5921135, essv6073810, essv6022569, essv6572666, essv5610629, essv5705935, essv5812242, essv6192165, essv6255638, essv6077938, essv6336960, essv5724424, essv5726631, essv6511633, essv6469037, essv5841775, essv6193238, essv6495036, essv5833944, essv5759200, essv5424307, essv6381981, essv5482588, essv5620799, essv5576629, essv5523436, essv5568916, essv6202472 | | Samples | NA12717, NA19058, NA20529, NA12842, NA18621, NA20766, NA11995, NA11829, NA19066, NA10851, NA12414, NA18561, NA12843, NA11920, NA11933, NA18599, NA18999, NA18603, NA12045, NA12751, NA12004, NA12058, NA12400, NA18633, NA20771, NA12750, NA18602, NA18988, NA12341, NA20814, NA20537, NA19068, NA19005, NA18940, NA18550, NA18597, NA18595, NA18635, NA20769, NA12348, NA18942, NA18618, NA19062, NA18574, NA11992, NA07048, NA07347, NA20768, NA12287, NA19054, NA18964, NA18949, NA20541, NA18611, NA12761, NA11930, NA20759, NA20518, NA20775, NA06984, NA11932, NA18560, NA11994, NA18557, NA12828, NA20755, NA18638, NA11993, NA20818, NA18605, NA20535, NA19082, NA19070, NA20787, NA20524, NA12342, NA18956, NA20810, NA20536, NA18579, NA12718, NA20519, NA18572, NA18630, NA18548, NA18566, NA18573, NA11893, NA11894, NA06989, NA19059, NA18536, NA12778, NA20542, NA18593, NA18541, NA19012, NA18546, NA20526, NA18632, NA18542, NA12716, NA18535, NA18559, NA12775, NA20815, NA18950, NA12272, NA20804, NA20520, NA20785, NA19010, NA12046, NA20530, NA20527, NA20504, NA19083, NA20803, NA20797, NA07037, NA12763, NA19085, NA18615, NA12347, NA06986, NA19078, NA18971, NA20582, NA19060, NA20510, NA18609, NA20826, NA18983, NA18984, NA18989, NA19004, NA18968, NA12006, NA18623, NA07000, NA18549, NA20754, NA19074, NA18622, NA12776, NA18577, NA20509, NA18620 | | Known Genes | ADCY8 | | 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) | esv2669733
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 148 | | Observed Complex | 0 | | Frequency | n/a |
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