Variant DetailsVariant: esv3617214Internal ID | 6657410 | Landmark | | Location Information | | Cytoband | 8q11.23 | Allele length | Assembly | Allele length | hg38 | 135641 | hg19 | 135641 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13200501, essv13200500 | Samples | HG00559, NA20806 | Known Genes | FAM150A, RB1CC1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3617214
| Frequency | Sample Size | 2504 | Observed Gain | 2 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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