Variant DetailsVariant: essv15475622Internal ID | 5477438 | Landmark | | Location Information | | Cytoband | 16q12.1 | Allele length | Assembly | Allele length | hg38 | 200440 | hg19 | 200440 |
| Variant Type | CNV gain | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3638608 | Supporting Variants | | Samples | NA19457 | Known Genes | CYLD, NOD2, SNX20 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | essv15475622
| Frequency | Sample Size | 2504 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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