Variant DetailsVariant: esv3606984Internal ID | 6647226 | Landmark | | Location Information | | Cytoband | 5q31.3 | Allele length | Assembly | Allele length | hg38 | 8194 | hg19 | 8194 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv12079230, essv12079232, essv12079229, essv12079231 | Samples | HG03515, NA18867, NA19247, HG01344 | Known Genes | PCDHGA1, PCDHGA2, PCDHGA3, PCDHGA4, PCDHGA5, PCDHGA6, PCDHGA7, PCDHGA8, PCDHGB1, PCDHGB2, PCDHGB3, PCDHGB4 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3606984
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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