Variant DetailsVariant: esv3617225Internal ID | 6657421 | Landmark | | Location Information | | Cytoband | 8q11.23 | Allele length | Assembly | Allele length | hg38 | 92847 | hg19 | 92847 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13201689, essv13201691, essv13201688, essv13201690 | Samples | HG01124, HG01444, HG03461, HG01491 | Known Genes | NPBWR1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3617225
| Frequency | Sample Size | 2504 | Observed Gain | 4 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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