Variant DetailsVariant: esv3643782Internal ID | 6683852 | Landmark | | Location Information | | Cytoband | 19p13.12 | Allele length | Assembly | Allele length | hg38 | 4071 | hg19 | 4071 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv16002656, essv16002659, essv16002662, essv16002663, essv16002665, essv16002664, essv16002654, essv16002666, essv16002658, essv16002653, essv16002657, essv16002655, essv16002660, essv16002668, essv16002667, essv16002661 | Samples | NA18980, HG00634, NA19062, NA18574, HG00543, NA18613, NA20299, NA18531, NA18535, NA18952, HG00707, HG02079, HG02032, NA18989, HG02020, HG02060 | Known Genes | CYP4F11 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3643782
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 16 | Observed Complex | 0 | Frequency | n/a |
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