Variant DetailsVariant: esv3624237 | Internal ID | 7011093 | | Landmark | | | Location Information | | | Cytoband | 10q23.33 | | Allele length | | Assembly | Allele length | | hg38 | 3990 | | hg19 | 3990 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv13899577, essv13899567, essv13899496, essv13899530, essv13899568, essv13899605, essv13899545, essv13899486, essv13899536, essv13899482, essv13899519, essv13899487, essv13899602, essv13899533, essv13899553, essv13899521, essv13899513, essv13899620, essv13899493, essv13899544, essv13899515, essv13899560, essv13899611, essv13899551, essv13899624, essv13899606, essv13899540, essv13899497, essv13899580, essv13899557, essv13899598, essv13899532, essv13899541, essv13899529, essv13899517, essv13899634, essv13899570, essv13899564, essv13899550, essv13899574, essv13899534, essv13899585, essv13899578, essv13899572, essv13899483, essv13899561, essv13899539, essv13899489, essv13899590, essv13899597, essv13899526, essv13899573, essv13899508, essv13899631, essv13899562, essv13899608, essv13899589, essv13899554, essv13899499, essv13899514, essv13899510, essv13899583, essv13899617, essv13899511, essv13899575, essv13899538, essv13899603, essv13899635, essv13899601, essv13899527, essv13899571, essv13899505, essv13899566, essv13899609, essv13899626, essv13899552, essv13899594, essv13899582, essv13899610, essv13899507, essv13899618, essv13899604, essv13899512, essv13899506, essv13899543, essv13899595, essv13899485, essv13899495, essv13899501, essv13899619, essv13899613, essv13899630, essv13899636, essv13899558, essv13899625, essv13899494, essv13899509, essv13899492, essv13899588, essv13899621, essv13899524, essv13899490, essv13899528, essv13899531, essv13899488, essv13899516, essv13899623, essv13899627, essv13899622, essv13899612, essv13899549, essv13899586, essv13899555, essv13899535, essv13899584, essv13899628, essv13899593, essv13899484, essv13899579, essv13899563, essv13899546, essv13899615, essv13899522, essv13899480, essv13899542, essv13899498, essv13899523, essv13899500, essv13899504, essv13899632, essv13899600, essv13899599, essv13899548, essv13899616, essv13899491, essv13899565, essv13899569, essv13899633, essv13899518, essv13899537, essv13899629, essv13899559, essv13899591, essv13899481, essv13899614, essv13899592, essv13899607, essv13899547, essv13899520, essv13899502, essv13899503, essv13899576, essv13899596, essv13899556, essv13899587, essv13899525, essv13899581 | | Samples | HG01850, HG00650, HG01795, HG01521, HG02072, NA18621, HG01443, HG01855, NA18561, HG02122, HG02029, NA19734, HG02078, NA18603, HG01806, HG01802, HG00566, NA18530, HG01809, NA19067, NA18988, HG01924, HG00337, NA18967, HG00622, HG01571, NA12812, HG02153, HG02016, NA18995, HG02087, HG00674, HG00448, HG02383, NA19723, HG02521, NA18558, HG01459, HG01843, HG00634, NA18960, HG02374, NA18642, HG01848, HG00537, NA19079, NA18611, HG03830, NA18749, HG01455, HG02252, NA18977, HG02389, NA19075, HG02082, HG00422, HG01973, HG02178, HG01932, NA18990, HG02073, NA18557, HG01709, HG00419, HG02164, HG01851, HG00675, NA18645, NA18614, HG00543, HG02402, HG01139, HG02136, HG01867, HG01841, NA20858, NA19070, HG01595, HG01857, HG01515, HG02253, HG00475, NA19717, HG02084, HG00436, HG01810, HG01845, HG01142, NA18637, HG02522, NA18948, HG01808, HG00619, HG02364, HG00651, HG03824, HG00844, NA19655, HG00690, HG00479, HG02048, HG02121, NA19752, HG02081, NA19009, HG02184, HG00704, NA18536, HG00410, NA18634, NA18593, HG02127, HG00445, NA18974, NA18546, HG01148, HG01858, HG00476, NA18533, HG01597, NA18543, NA18628, HG02064, HG01800, HG02391, HG01977, HG01598, NA19786, NA19741, HG02137, HG02128, NA18631, HG02367, HG01028, NA18987, HG02032, HG01846, HG02396, HG01254, NA18636, HG02291, NA18972, HG01468, HG00728, HG01794, NA19661, HG01807, HG00472, NA18989, HG01125, NA18968, HG00759, NA18549, HG02406, HG01923, NA18620, HG01926 | | Known Genes | | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3624237
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 157 | | Observed Complex | 0 | | Frequency | n/a |
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