Variant DetailsVariant: esv3640934Internal ID | 6681019 | Landmark | | Location Information | | Cytoband | 17q23.2 | Allele length | Assembly | Allele length | hg38 | 10546 | hg19 | 10546 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15716223, essv15716225, essv15716226, essv15716224, essv15716222 | Samples | HG03821, HG04094, HG03673, HG04062, HG03741 | Known Genes | BCAS3 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3640934
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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