Variant DetailsVariant: esv3637921Internal ID | 6678020 | Landmark | | Location Information | | Cytoband | 16p13.13 | Allele length | Assembly | Allele length | hg38 | 3387 | hg19 | 3387 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15375165, essv15375163, essv15375166, essv15375168, essv15375164, essv15375161, essv15375162, essv15375169, essv15375167, essv15375160 | Samples | NA18749, HG03132, HG02397, HG00436, NA18533, NA18559, HG04141, NA18631, HG04153, HG00593 | Known Genes | CLEC16A | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3637921
| Frequency | Sample Size | 2504 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|