Variant DetailsVariant: esv2661063 | Internal ID | 2894150 | | Landmark | | | Location Information | | | Cytoband | 5q32 | | Allele length | | Assembly | Allele length | | hg38 | 426 | | hg19 | 426 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv5793004, essv5840898, essv6450368, essv5531739, essv6488186, essv5838785, essv5962029, essv5565677, essv6101527, essv6284916, essv6031718, essv5906415, essv5944202, essv6302412, essv6472837, essv5423442, essv6079364, essv5871145, essv5537464, essv5577664, essv5578740, essv5851337, essv6592476, essv5508725, essv6108473, essv6122809, essv6587208, essv6321846, essv6286696, essv5544191, essv5578428, essv5849050, essv5549914, essv6227368, essv5519361, essv6401034, essv5545512, essv6075908, essv6556924, essv5646997, essv6538863, essv5892083, essv6467322, essv6255421, essv6062241, essv5675941, essv5470490, essv6241136, essv6435531, essv6473371, essv5511173, essv6344600, essv6469943, essv5463380, essv6360543, essv5999133, essv5692654, essv6454383, essv5583970, essv6555986, essv6156643, essv6002667, essv6556666, essv5723476, essv6192638, essv6104388, essv5764867, essv5430715, essv5716323, essv6431672, essv6281861, essv5714974, essv6352174, essv5858859, essv6289911, essv6124606, essv6188701, essv6140446, essv6148335, essv6528234, essv6168174, essv6040002, essv5908937, essv5479337, essv6541947, essv5569983, essv5749160, essv6098942, essv6007718, essv6039110, essv6209756, essv6207774, essv5534272, essv5977484, essv5480461, essv6258918, essv5971070, essv6141940, essv6565081, essv5450920, essv5678343, essv6544414, essv5915808, essv6326531, essv5867004, essv6136848, essv6016998, essv5445130, essv5620087, essv5472981, essv5397382, essv5815554, essv5979396, essv5701844, essv5594332, essv6286809, essv6553354, essv6488222, essv5790207, essv6493375, essv5747982, essv6166451, essv5878842, essv5883512, essv5645314, essv5899269, essv5913827, essv5954103, essv6507273, essv6130865, essv6220169, essv5870041, essv5430427, essv5433364, essv5803110, essv5904407, essv5857070, essv5649854, essv6355750, essv5727234, essv5601477, essv5524458, essv5623601, essv5737706, essv5445348, essv6275300, essv5977989, essv5681706, essv6320676, essv6241510, essv5851144, essv6100423, essv6500358, essv6500379, essv6497885, essv5771299, essv6177193, essv6020113, essv6232754, essv6116736, essv6414777, essv5678494, essv5913316, essv6357239, essv5433539, essv6197407, essv5590575, essv5927733, essv5908727, essv5697159, essv5754819, essv5761775, essv6482415, essv5456374, essv6435930, essv6209308, essv6572207, essv6422357, essv5491653, essv6474312, essv5528216, essv5712696, essv6001212, essv5658836, essv6304344, essv5432589, essv5839106, essv6041094, essv5524904, essv5996831, essv6288651, essv5437420, essv5903949, essv6015807, essv5602701, essv6168722, essv5928358, essv5532273, essv5769147, essv6379182, essv5439426, essv5528409, essv6539312, essv6394142, essv6086532, essv5572458, essv5451183, essv5792371, essv5853533, essv5424728, essv6488024, essv5964395, essv6130112, essv6040622, essv6183432, essv5909823 | | Samples | HG01441, NA19012, NA19137, NA12827, NA18621, NA18964, NA19312, NA19152, HG00152, HG01359, HG00252, HG00536, NA07347, NA20787, HG00257, NA18520, NA07037, NA18951, NA19321, NA20809, NA18871, NA20785, HG01052, NA12342, HG01342, NA20516, HG00500, NA11920, HG00464, HG00131, NA19783, NA20544, NA20531, NA11918, NA19469, NA18550, HG00707, NA20299, NA10847, NA20802, HG01389, NA19670, HG00657, NA12813, HG00117, HG00577, NA19788, HG01492, NA20800, HG01491, NA18573, NA18608, NA19920, NA18542, HG00553, HG01350, HG00139, NA19379, NA18507, NA20588, HG00111, NA12776, NA19685, HG01461, NA07051, NA19648, HG00651, HG00335, HG00557, NA19257, NA19701, NA19084, NA20755, NA12044, HG01551, NA18873, NA19776, NA19438, NA19654, NA19762, NA19726, NA19914, NA20761, HG00242, NA18912, NA19085, HG00179, HG00593, NA12282, HG01375, NA19652, HG00337, NA11994, NA18635, NA19068, NA18536, NA19660, HG00140, NA18622, NA18618, NA20504, HG00610, HG01061, HG00692, HG01047, NA20807, HG01124, NA18592, NA20127, HG00330, NA07048, NA19429, NA20541, NA20765, NA18547, NA19985, NA12829, NA19256, HG01113, NA11894, NA20520, NA19773, NA19658, NA19681, NA19663, NA19679, NA19457, HG00357, NA19700, NA19082, HG00584, HG00114, NA12751, NA19000, NA19213, NA19725, NA19313, NA19380, HG01111, HG01437, NA19153, HG00124, NA12716, NA18620, HG01465, HG00233, HG01066, NA12778, NA19373, HG00325, NA20790, HG00185, NA18486, NA19102, HG00263, NA18522, NA19238, HG00560, NA19713, HG01073, NA19098, NA19664, HG00501, HG00249, NA18961, HG01080, NA19909, NA20797, HG00524, NA19720, HG00512, NA19159, NA19382, HG01383, NA18579, HG01094, NA18619, NA20525, HG00595, NA19138, NA19391, NA19723, NA19201, HG00611, HG00650, HG00663, NA12156, NA12889, HG00580, HG00448, NA19755, HG01390, NA19452, NA20513, HG00530, HG00285, NA19717, NA12546, NA11932, HG01177, HG01498, NA19204, NA19350, HG01489, NA19079, NA19381, NA18615, NA19758, HG00476, NA20538, HG00702, HG00271, NA18519, NA19746, HG01067, HG01198 | | Known Genes | CSF1R | | Method | Merging | | Analysis | No reference, merging analysis | | Platform | Merging | | Comments | High quality site | | Reference | 1000_Genomes_Consortium_Phase_1 | | Pubmed ID | 23128226 | | Accession Number(s) | esv2661063
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 216 | | Observed Complex | 0 | | Frequency | n/a |
|
|
