Variant DetailsVariant: esv2672420 Internal ID | 9591839 | Landmark | | Location Information | | Cytoband | 10p12.1 | Allele length | Assembly | Allele length | hg38 | 300 | hg19 | 300 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5471252, essv5784273, essv6273914, essv6428517, essv6473262, essv5983082, essv5440236, essv6001108, essv5889338, essv6036896, essv6086553, essv6164904, essv5868711, essv6593209, essv6015477, essv6230973, essv5993450, essv6381881, essv5598008, essv5398861, essv5616135, essv5598453, essv6498823, essv5548122, essv5834652, essv6098050, essv5821347, essv5664650, essv6474268, essv5932682, essv5582099, essv5455416, essv6558161, essv5552446 | Samples | HG01079, HG00640, NA19359, NA12004, NA20517, HG01350, NA19005, NA20589, NA20795, NA12761, NA20759, NA12275, HG00236, HG00325, NA12828, HG00253, NA11993, HG00108, HG01136, HG00188, NA19210, HG01171, NA20810, NA19327, HG00250, NA12892, HG01204, NA12716, NA19712, HG00638, NA20804, NA19144, NA19129, NA18511 | Known Genes | MPP7 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2672420
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 34 | Observed Complex | 0 | Frequency | n/a |
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