Variant DetailsVariant: esv3645582Internal ID | 6685644 | Landmark | | Location Information | | Cytoband | 20p11.21 | Allele length | Assembly | Allele length | hg38 | 33753 | hg19 | 33753 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv16166456, essv16166457 | Samples | HG00629, HG00266 | Known Genes | ABHD12, PYGB | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3645582
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
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