Variant DetailsVariant: esv2658549 Internal ID | 9577968 | Landmark | | Location Information | | Cytoband | 10p15.3 | Allele length | Assembly | Allele length | hg38 | 122 | hg19 | 122 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6503138, essv6497794, essv6493195, essv5605804, essv5825386, essv5432953, essv5916622, essv6583329, essv5926088, essv6329614, essv6331135, essv6362550, essv6216071, essv6195833, essv6021941, essv5863486, essv5907221, essv5696033, essv5841510, essv6090773, essv6147385, essv6084197, essv6265835, essv6571467, essv5923030, essv6075191, essv5982190, essv6355386, essv6418041, essv6344150, essv6061086, essv5867577, essv6555725, essv6551453, essv5737075, essv6330660, essv6219191, essv6161755, essv6007962, essv6470568, essv5881503, essv6250106, essv5652887, essv6017722, essv5699346, essv6185481, essv6412964, essv6595527, essv6581070, essv5708328, essv5928852, essv6506389, essv5952854, essv5957870, essv5500970, essv5466550, essv6266468, essv6206407, essv5934368, essv5588282, essv6275788, essv5707562, essv5593423, essv6445411, essv6140555, essv5639655, essv6585210, essv5728700, essv5999641, essv5925658, essv6236642, essv6383150, essv6287852, essv6399970, essv5861937, essv5692605, essv5929189, essv6385831, essv6080384, essv5980172, essv6485149, essv6060072, essv6326523, essv6204135, essv5586470, essv5460469, essv5417948, essv5686023, essv5465207, essv6288859, essv6225170, essv6524650, essv6198853, essv6358310, essv6425347, essv5444259, essv5566048, essv6197742, essv6109342, essv6324412, essv5572541, essv6383368, essv5813683, essv6561349, essv5924801, essv5856340, essv5489983, essv5590743, essv6462620, essv5687215, essv5578885, essv6414228, essv6368089, essv5611314, essv6410097, essv6473862, essv6480363, essv5945494, essv6022786, essv6127907, essv5541877, essv5498846, essv5423559 | Samples | HG00650, HG00442, NA11830, HG01173, HG00536, HG00608, NA18621, HG00249, HG00671, HG00524, NA18561, NA11933, NA18599, HG00699, NA18530, NA18606, NA18633, NA18602, HG00693, HG00337, HG00271, HG00663, NA18940, HG01366, HG00589, HG00702, HG00689, HG00448, NA18619, HG00346, NA18582, NA19457, NA20513, HG00537, HG00590, HG00512, HG01069, HG00325, HG00534, HG00422, HG00705, NA19087, HG00309, HG00427, NA18557, NA20342, NA19445, HG00326, HG00323, HG00530, HG00419, HG00108, HG01353, HG00543, HG00313, HG01183, HG00154, NA18605, NA18613, HG00443, HG00428, HG00475, HG00436, HG00556, HG00584, HG00533, NA18637, HG00500, HG00275, NA18572, NA18534, HG00619, HG00708, HG00692, NA18548, HG00284, HG00479, NA18532, HG00613, HG00525, NA12827, HG00704, HG00463, HG01107, NA18576, NA18632, HG00476, HG00254, NA18543, NA18559, NA19749, HG00353, NA19072, HG00580, HG01357, HG00473, HG00237, HG01108, HG00662, HG00418, HG00620, HG00125, HG00707, HG00672, HG00614, HG00111, HG00513, HG00478, HG00421, HG00656, NA18609, HG00280, HG01377, HG00472, HG01378, HG01082, NA18623, NA18612, NA18622, HG00437, NA18562, HG00581, NA18620 | Known Genes | ADARB2 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2658549
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 123 | Observed Complex | 0 | Frequency | n/a |
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