Variant DetailsVariant: esv3588641 | Internal ID | 6976057 | | Landmark | | | Location Information | | | Cytoband | 1q32.1 | | Allele length | | Assembly | Allele length | | hg38 | 975 | | hg19 | 975 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv10271288, essv10271301, essv10271253, essv10271324, essv10271200, essv10271232, essv10271345, essv10271277, essv10271228, essv10271221, essv10271278, essv10271248, essv10271276, essv10271214, essv10271287, essv10271272, essv10271270, essv10271195, essv10271283, essv10271327, essv10271311, essv10271275, essv10271308, essv10271243, essv10271342, essv10271318, essv10271245, essv10271307, essv10271196, essv10271234, essv10271252, essv10271220, essv10271213, essv10271233, essv10271295, essv10271210, essv10271208, essv10271292, essv10271310, essv10271321, essv10271236, essv10271262, essv10271312, essv10271197, essv10271316, essv10271306, essv10271204, essv10271194, essv10271328, essv10271317, essv10271282, essv10271291, essv10271289, essv10271286, essv10271269, essv10271237, essv10271305, essv10271332, essv10271223, essv10271294, essv10271273, essv10271240, essv10271337, essv10271239, essv10271257, essv10271235, essv10271280, essv10271274, essv10271230, essv10271264, essv10271256, essv10271201, essv10271205, essv10271331, essv10271329, essv10271284, essv10271299, essv10271247, essv10271325, essv10271268, essv10271263, essv10271322, essv10271340, essv10271241, essv10271341, essv10271224, essv10271303, essv10271218, essv10271315, essv10271279, essv10271199, essv10271296, essv10271191, essv10271304, essv10271285, essv10271281, essv10271336, essv10271251, essv10271216, essv10271333, essv10271215, essv10271339, essv10271225, essv10271209, essv10271258, essv10271244, essv10271313, essv10271293, essv10271202, essv10271231, essv10271320, essv10271217, essv10271260, essv10271297, essv10271222, essv10271211, essv10271338, essv10271206, essv10271192, essv10271242, essv10271255, essv10271207, essv10271203, essv10271314, essv10271212, essv10271193, essv10271300, essv10271254, essv10271238, essv10271298, essv10271227, essv10271226, essv10271250, essv10271190, essv10271335, essv10271309, essv10271198, essv10271330, essv10271323, essv10271261, essv10271319, essv10271334, essv10271219, essv10271290, essv10271249, essv10271265, essv10271271, essv10271266, essv10271344, essv10271267, essv10271343, essv10271302, essv10271259, essv10271246, essv10271229, essv10271326 | | Samples | NA19214, HG03166, HG03265, NA19394, HG02614, HG01986, HG02574, HG02339, HG01413, HG02890, NA19141, HG02628, NA19703, HG03378, NA18861, HG03163, HG03175, NA19378, HG02337, NA18877, HG02891, NA18486, HG03298, HG03280, NA20294, NA19393, NA18878, HG03100, NA19377, HG03515, HG03139, HG03577, HG02888, NA19920, HG03069, HG02769, HG03095, NA19446, NA19374, HG03436, NA18519, HG03385, HG03168, HG03099, HG02810, NA18489, NA19728, HG03499, NA19307, NA19198, HG03485, HG02620, HG03370, HG02860, HG03342, NA20287, HG03040, NA19904, NA20291, HG02562, NA20278, HG03556, NA18874, HG03268, NA18868, HG03212, HG02642, NA19159, HG02502, NA19189, NA19239, NA18864, HG02623, NA19456, NA19445, HG03583, NA20127, NA18908, HG03114, HG02882, HG02715, HG03048, HG02716, HG03120, HG03132, HG03363, NA19707, NA19462, HG02449, NA19327, NA19913, HG02450, HG03428, HG01989, HG02307, NA18910, HG03159, HG01880, HG02497, HG02470, HG02555, HG01092, HG03301, HG03085, HG02445, HG03397, HG02884, NA18853, HG03046, HG02666, HG03354, HG02586, HG02594, NA18858, HG01990, NA19308, HG03028, NA19309, HG02282, NA19390, NA18909, HG03240, NA19108, HG03437, HG02799, HG02546, HG02611, HG02314, HG03469, HG02941, NA19310, HG03304, NA20281, HG02558, NA18501, HG02971, HG02970, HG01556, HG03313, HG03049, HG02107, HG01055, HG03258, HG03351, NA19096, HG03538, NA19900, HG01914, NA19030, NA18505, HG02855, NA18488, NA19312, HG03376, HG03198, HG03303 | | Known Genes | | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3588641
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 156 | | Observed Complex | 0 | | Frequency | n/a |
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