Variant DetailsVariant: esv3588715 | Internal ID | 6976131 | | Landmark | | | Location Information | | | Cytoband | 1q32.2 | | Allele length | | Assembly | Allele length | | hg38 | 4767 | | hg19 | 4767 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv10284413, essv10284444, essv10284442, essv10284391, essv10284383, essv10284388, essv10284456, essv10284447, essv10284359, essv10284363, essv10284453, essv10284394, essv10284450, essv10284407, essv10284420, essv10284466, essv10284415, essv10284425, essv10284387, essv10284467, essv10284368, essv10284379, essv10284434, essv10284356, essv10284374, essv10284465, essv10284401, essv10284404, essv10284432, essv10284422, essv10284392, essv10284393, essv10284454, essv10284451, essv10284377, essv10284373, essv10284406, essv10284439, essv10284468, essv10284443, essv10284365, essv10284355, essv10284369, essv10284402, essv10284411, essv10284360, essv10284460, essv10284371, essv10284438, essv10284441, essv10284440, essv10284416, essv10284372, essv10284375, essv10284461, essv10284418, essv10284357, essv10284421, essv10284366, essv10284364, essv10284408, essv10284370, essv10284427, essv10284385, essv10284435, essv10284417, essv10284381, essv10284458, essv10284445, essv10284395, essv10284400, essv10284464, essv10284409, essv10284362, essv10284436, essv10284396, essv10284382, essv10284405, essv10284386, essv10284463, essv10284378, essv10284361, essv10284459, essv10284431, essv10284390, essv10284399, essv10284384, essv10284414, essv10284437, essv10284433, essv10284397, essv10284398, essv10284462, essv10284380, essv10284457, essv10284424, essv10284419, essv10284446, essv10284428, essv10284376, essv10284423, essv10284426, essv10284358, essv10284412, essv10284455, essv10284452, essv10284403, essv10284389, essv10284448, essv10284367, essv10284430, essv10284449, essv10284354, essv10284429, essv10284410 | | Samples | HG01985, HG01485, NA20339, NA19700, HG03484, NA19399, HG02702, HG02433, HG03300, HG02419, NA20321, NA20298, NA19819, NA19393, HG02536, NA19443, NA19920, HG02895, NA18519, HG02621, HG02811, NA19315, NA18489, NA19448, NA19198, NA19916, NA19131, HG03342, HG03246, HG03105, NA18498, HG01242, HG02489, NA19922, HG02143, HG02561, HG03189, HG03212, NA19372, NA19024, HG02471, NA19026, NA19901, HG02502, NA20355, HG03267, HG03114, HG03048, HG02879, HG02479, HG03120, HG02977, HG03363, HG01435, HG03061, NA19462, HG02678, NA19984, HG03547, NA19391, NA19455, NA19236, HG02953, HG02307, NA18871, HG03081, HG02968, HG02497, HG02976, HG03294, NA18907, HG01390, NA19774, NA19449, HG03382, HG02884, HG03571, HG02585, HG02635, HG02568, HG01956, NA19206, HG03461, NA19256, HG02799, HG02759, HG03539, HG02983, HG01272, NA19380, HG02611, HG01375, HG03127, HG03304, HG02771, HG02970, HG01912, HG03049, NA19713, HG03258, NA20289, HG03401, HG02052, HG01883, NA18505, NA19312, HG02284, HG03198, HG02808, HG03118, NA19346, NA19153, NA19431, HG03196, HG02760 | | Known Genes | SYT14 | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3588715
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 115 | | Observed Complex | 0 | | Frequency | n/a |
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