Variant DetailsVariant: esv3635296Internal ID | 6675409 | Landmark | | Location Information | | Cytoband | 14q32.11 | Allele length | Assembly | Allele length | hg38 | 5042 | hg19 | 5042 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15093039, essv15093036, essv15093037, essv15093038, essv15093035 | Samples | HG02727, HG03792, NA21105, HG03875, HG03779 | Known Genes | FOXN3 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3635296
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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