Variant DetailsVariant: esv3637615Internal ID | 6677718 | Landmark | | Location Information | | Cytoband | 16p13.3 | Allele length | Assembly | Allele length | hg38 | 8233 | hg19 | 8233 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv473e214 | Supporting Variants | essv15359755, essv15359754, essv15359753, essv15359756, essv15359752 | Samples | HG03517, HG02922, HG00629, HG00266, HG03511 | Known Genes | GNPTG, UNKL | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3637615
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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