Variant DetailsVariant: esv3608791Internal ID | 6649024 | Landmark | | Location Information | | Cytoband | 6p21.1 | Allele length | Assembly | Allele length | hg38 | 1389 | hg19 | 1389 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv12327732, essv12327729, essv12327728, essv12327726, essv12327731, essv12327730, essv12327727 | Samples | NA20321, NA20320, NA19138, NA19025, HG02450, HG03301, HG03118 | Known Genes | FOXP4 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3608791
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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