Variant DetailsVariant: esv2664817 Internal ID | 9584236 | Landmark | | Location Information | | Cytoband | 13q14.13 | Allele length | Assembly | Allele length | hg38 | 8548 | hg19 | 8548 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5481604, essv5753142, essv6195225, essv5721567, essv6364707, essv6153617, essv5448288, essv5642056, essv5722249, essv6479115, essv6462002, essv5684752, essv6548188, essv6079859, essv5598513, essv6102120, essv6416493, essv5844640, essv6387189, essv6518868, essv5827660, essv5823617, essv6231558, essv5508523, essv6504589, essv6532612, essv5750458, essv5997139, essv5689234, essv5639746, essv5794935, essv5894031, essv6038822, essv6226868, essv5929773, essv5894555, essv5988734, essv5779650, essv6201906, essv5964519, essv6114056, essv6024697, essv5851079, essv6294428, essv5986356, essv6597840, essv5829220, essv5430051, essv5490384, essv5874073, essv6004180, essv5437398, essv5934807, essv5980072, essv5961175, essv5771155, essv5940303, essv6490440, essv6187006, essv5420747, essv6156577, essv5999132, essv5674306, essv5772372, essv6196350, essv5917227, essv5805672, essv5860541, essv5875781, essv6453485, essv6542473, essv6158407, essv6368762, essv5416611, essv5733471, essv5955335, essv6312020, essv5480564, essv6228323, essv6545393 | Samples | HG00613, HG00537, HG00607, HG00619, HG00705, HG00437, HG00500, HG00596, HG00565, HG00707, HG00463, HG00657, HG01488, HG00428, HG00475, HG00542, HG00683, HG00404, HG01461, HG00651, HG00557, HG00578, HG00479, HG00592, HG00543, HG01550, HG00556, HG01140, HG00593, HG01375, HG00583, HG00692, HG01495, HG00689, HG01124, HG00628, HG00533, HG00419, HG01253, HG00634, HG00403, HG00584, HG00620, HG01437, HG01465, HG00653, HG00629, HG00559, HG00560, HG00672, HG00513, HG00524, HG00534, HG01383, HG01149, HG00427, HG00590, HG00595, HG00611, HG00663, HG00580, HG01112, HG00448, HG00654, HG01366, HG00708, HG00566, HG01498, HG00625, HG00442, HG00473, HG01462, HG01489, HG00626, HG00684, HG00476, HG00671, HG00704, HG00531, HG01354 | Known Genes | | 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) | esv2664817
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 80 | Observed Complex | 0 | Frequency | n/a |
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