Variant DetailsVariant: esv3622742 Internal ID | 6662911 | Landmark | | Location Information | | Cytoband | 10p12.1 | Allele length | Assembly | Allele length | hg38 | 8051 | hg19 | 8051 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13737827, essv13737830, essv13737845, essv13737832, essv13737829, essv13737841, essv13737836, essv13737831, essv13737838, essv13737833, essv13737846, essv13737839, essv13737844, essv13737826, essv13737825, essv13737847, essv13737842, essv13737837, essv13737843, essv13737828, essv13737834, essv13737840, essv13737835, essv13737848 | Samples | HG02339, HG03484, NA19332, HG02012, HG03280, NA19446, HG00641, NA18489, NA19457, HG03055, NA19908, NA19437, HG03132, HG01879, HG03123, NA18856, HG01182, HG02330, NA19108, NA19149, HG01205, NA19093, HG03162, HG03271 | Known Genes | MPP7 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3622742
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 24 | Observed Complex | 0 | Frequency | n/a |
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