Variant DetailsVariant: esv2657528 | Internal ID | 9923633 | | Landmark | | | Location Information | | | Cytoband | 8q23.1 | | Allele length | | Assembly | Allele length | | hg38 | 1546 | | hg19 | 1546 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | dgv1301e199 | | Supporting Variants | essv5415999, essv5426306, essv6066492, essv5564795, essv6149694, essv5894112, essv5754072, essv6330344, essv6007415, essv6205882, essv5871086, essv6152439, essv5525101, essv5470395, essv6008896, essv5986103, essv6386346, essv5830345, essv6478332, essv5416534, essv6330290, essv5501735, essv5897101, essv6143979, essv6183229, essv6127044, essv6593102, essv6389197, essv6233525, essv6409144, essv6066309, essv5420174, essv6529624, essv5600760, essv5575113, essv6448987, essv5400538, essv6414851, essv5980771, essv6032295, essv6262595, essv6201547, essv6369697, essv5706258, essv6202681, essv5450072, essv5938290, essv5686529, essv5726931, essv5452422, essv6380567, essv5483260, essv5481659, essv5419311, essv6359819, essv5681094, essv6438131, essv6310637, essv6288479, essv5967474, essv6171736, essv6227671, essv5804066, essv6502764, essv6401481, essv6077374, essv5635388, essv5515770, essv5689118, essv6026901, essv5458376, essv6439433, essv5640441, essv6486508, essv5951208, essv5513199, essv6007588, essv6443256, essv6420023, essv6204181, essv5767143, essv5416284, essv6306800, essv5939417, essv5798000, essv5576394, essv5508346, essv5617283, essv6457527, essv6459463, essv5597521, essv6590033, essv6431110, essv5506494, essv6402613, essv5892008, essv5924784 | | Samples | NA18502, NA20761, NA12842, HG00536, NA19664, NA19466, NA18980, HG01389, HG01465, NA19777, NA18616, HG01518, HG00177, NA19443, NA20806, NA19067, NA19746, HG00251, NA20589, HG01351, NA18558, HG00610, NA18574, HG00247, NA20336, HG00243, NA20291, NA19079, NA19651, HG01067, HG00683, HG00106, NA19137, NA19371, HG00705, NA19725, HG01133, NA20533, NA18908, NA19007, NA12777, HG00731, HG00557, NA19077, HG00428, HG00732, HG00653, NA19236, HG00344, HG01498, NA19788, NA18579, NA18871, HG01149, NA18534, NA19776, HG00740, HG01047, NA18566, HG00651, HG01197, NA18499, NA19453, HG00525, NA12827, HG01334, NA18858, NA18593, NA19012, NA12043, NA18608, HG00124, HG00336, NA18961, NA18559, NA19434, HG00375, HG00638, HG00278, NA07051, NA20785, NA19010, NA19470, NA19085, NA18615, NA06986, NA19078, NA12749, NA20334, NA19711, HG01377, NA18984, NA18989, NA12006, NA19065, NA19074, HG00553 | | Known Genes | ANGPT1 | | 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) | esv2657528
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 97 | | Observed Complex | 0 | | Frequency | n/a |
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