Variant DetailsVariant: esv3638324Internal ID | 6678422 | Landmark | | Location Information | | Cytoband | 16p12.1 | Allele length | Assembly | Allele length | hg38 | 14815 | hg19 | 14815 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15439419, essv15439412, essv15439410, essv15439411, essv15439414, essv15439417, essv15439413, essv15439416, essv15439418, essv15439415 | Samples | HG00143, NA12004, HG01670, HG00324, HG00117, HG00336, HG03488, HG02235, HG01089, HG00112 | Known Genes | IL4R | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3638324
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
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