Variant DetailsVariant: esv3622400Internal ID | 6662570 | Landmark | | Location Information | | Cytoband | 10p13 | Allele length | Assembly | Allele length | hg38 | 974 | hg19 | 974 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13700159, essv13700161, essv13700165, essv13700163, essv13700160, essv13700162, essv13700164, essv13700166, essv13700167, essv13700168, essv13700169 | Samples | HG03559, NA18504, NA19171, HG02885, HG02571, HG01879, HG02613, NA19440, HG03461, HG03539, HG02771 | Known Genes | UCMA | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3622400
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 11 | Observed Complex | 0 | Frequency | n/a |
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