Variant DetailsVariant: esv2664309Internal ID | 9583728 | Landmark | | Location Information | | Cytoband | 9q32 | Allele length | Assembly | Allele length | hg38 | 6778 | hg19 | 6778 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6110345, essv5820382, essv6050195, essv6378935, essv6259598, essv5514044, essv5473220, essv5511682, essv6166534, essv6353635, essv6508395, essv5716345, essv6286305, essv6332283, essv5465739, essv6486608, essv6152251, essv5980867, essv6192823, essv5625509, essv5420673, essv6343511, essv5737090, essv6095908, essv5972525, essv5725163, essv6544604, essv5639488, essv6474163, essv5530629, essv5420354, essv5417560, essv5562233, essv6393823, essv5741579, essv6350609, essv6497821, essv5599962, essv6109615, essv5895947, essv5995739, essv6576384, essv6363637, essv6551930, essv6041543, essv6576705, essv5467032, essv6026759, essv5645896, essv6146364, essv6506561, essv6231800, essv5542444, essv5482036, essv6214500, essv5442425, essv5533624, essv6230895, essv6090481, essv6459781, essv6119472, essv6291062, essv5802978, essv6309145, essv6020781, essv6092631, essv6221587, essv5686668, essv6244564, essv5483450, essv5498790, essv6199291, essv6007895, essv5832716, essv6479381, essv5515846, essv6538988, essv6502179, essv5679451, essv5779200, essv6396554, essv6031356, essv5585524, essv6582759, essv6489628, essv5952005, essv5926144, essv5821496, essv6204528, essv5568175 | Samples | NA20529, NA19397, HG00249, NA19466, NA19399, HG01052, NA19332, NA19704, HG01389, HG01374, NA20816, NA19350, NA19355, NA19777, NA19684, NA19377, HG01461, NA19443, NA12399, NA19107, HG00663, NA19396, NA19381, NA19373, NA19076, NA19382, NA18489, NA19448, NA19678, HG01083, HG00369, NA19904, NA18874, NA18868, NA19372, NA19471, NA19901, NA18520, NA19456, NA18908, NA18867, NA19451, NA18934, HG01384, NA19347, NA19717, NA19236, NA19982, HG00500, NA20344, HG01390, HG01073, NA19453, NA18853, HG00152, NA19318, HG01107, NA18945, NA20765, NA19401, NA19440, NA19390, NA18535, NA19147, NA18559, NA19434, NA19473, NA19072, NA07051, NA19439, NA19428, NA19360, NA20341, NA19248, NA19472, NA19468, NA19093, NA20289, NA18873, NA19080, NA19711, NA19213, HG00343, NA19900, HG00595, NA19312, HG00345, NA19463, NA19346, NA18487 | Known Genes | ORM1, ORM2 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2664309
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 90 | Observed Complex | 0 | Frequency | n/a |
|
|