Variant DetailsVariant: esv2662333 | Internal ID | 9928438 | | Landmark | | | Location Information | | | Cytoband | 10q21.3 | | Allele length | | Assembly | Allele length | | hg38 | 2420 | | hg19 | 2420 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | dgv150e199 | | Supporting Variants | essv5680355, essv5406158, essv5576009, essv6384185, essv5938544, essv5554016, essv6022311, essv5504926, essv5839375, essv6355838, essv6265415, essv5608156, essv6289432, essv6371357, essv5777363, essv5477090, essv6054877, essv5791829, essv6371402, essv6296259, essv6075476, essv6564638, essv6318986, essv6228900, essv5816314, essv5654230, essv6231043, essv6153777, essv6473104, essv5846754, essv5996548, essv6271376, essv5952266, essv5702590, essv6503976, essv6588307, essv6109488, essv6085465, essv5992119, essv6089717, essv6558030, essv5601256, essv5886212, essv5397525, essv5507369, essv6364598, essv5884272, essv5933409, essv6110176, essv5708401, essv6511434, essv5547110, essv5897686, essv6419988, essv6112606, essv6563564, essv6390677, essv5469091, essv5484200, essv5566023, essv6476640, essv6267256, essv6048146, essv5459270, essv6496259, essv5890559, essv6563999, essv6002866, essv6074012, essv6344403, essv5767555, essv5689185, essv5457529, essv6563154, essv6277857, essv6308390, essv6202343, essv6352807, essv5921866, essv5564452, essv6430328, essv5906169, essv5754703, essv5793503, essv6120498, essv5478273, essv6596970, essv6462557, essv5754405, essv5528918, essv5470476, essv5654759, essv6598401, essv6542045, essv6066348, essv6096725, essv5751211, essv5695420, essv5651776, essv6377502, essv5615896, essv5501003, essv6421478, essv6100472, essv5728022, essv5478919, essv6103042, essv6496254, essv5925131, essv5967507, essv6126876, essv6459189, essv6004085, essv6461737, essv6329833, essv5704500, essv5667161, essv5476545, essv5718016, essv5437415, essv5818963, essv6059027, essv6134184, essv5501016, essv5805267, essv6507443, essv6156411, essv6520659, essv5566919, essv6082056, essv5561222, essv6581931, essv6048612, essv5572581, essv5538124, essv6154784, essv5949920, essv5916907, essv6314934 | | Samples | HG00650, HG00442, NA19055, HG00536, NA20766, HG00249, NA19664, NA11829, NA18592, HG00524, NA18980, NA18561, HG01389, HG00181, NA18959, NA18606, NA19920, NA18633, NA07357, NA19067, NA12341, NA19379, NA18940, NA18550, NA19201, HG00501, HG00448, NA19723, NA19119, NA18982, NA18635, NA18567, NA18618, NA18582, NA19771, NA18571, NA19782, NA19384, NA18964, HG00537, NA19079, HG00512, NA19720, NA20518, HG00683, NA18868, NA19917, NA19719, NA19137, HG00422, NA19189, NA18990, NA18520, NA18557, HG00419, NA19789, NA19451, NA18614, NA18544, NA19908, NA18613, NA20800, NA18538, HG00183, HG01187, HG00282, NA19070, NA19056, NA20524, HG00557, NA19717, HG00556, HG00584, NA18637, HG00500, NA18579, NA19658, NA18630, HG00635, NA18548, NA19654, NA18573, NA11919, NA18626, HG00690, HG00531, NA18963, HG00463, NA18593, HG01107, HG01204, NA18974, NA18953, NA18632, NA18542, NA19440, NA18543, NA19147, NA18559, NA18517, NA19712, NA18564, NA19747, NA18628, HG00580, NA19732, NA19435, NA07051, NA19334, NA20792, HG01494, NA19470, NA19311, HG01137, NA19083, NA07037, NA19783, HG00662, NA18610, NA19398, HG00707, HG00478, NA19248, NA18971, HG01491, NA18631, NA19779, NA19093, NA12830, HG00377, NA19661, HG00595, NA19755, NA18488, NA19312, NA18968, NA18624, NA18965, NA18620 | | Known Genes | PBLD | | Method | Merging | | Analysis | No reference, merging analysis | | Platform | Merging | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_1 | | Pubmed ID | 23128226 | | Accession Number(s) | esv2662333
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 139 | | Observed Complex | 0 | | Frequency | n/a |
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