Variant DetailsVariant: esv3644996Internal ID | 6685059 | Landmark | | Location Information | | Cytoband | 20p13 | Allele length | Assembly | Allele length | hg38 | 2079 | hg19 | 2079 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv16119031, essv16119028, essv16119032, essv16119025, essv16119027, essv16119033, essv16119029, essv16119030, essv16119026, essv16119024 | Samples | HG03548, HG03057, HG02836, HG03478, HG03086, HG02537, HG00740, HG03391, HG03469, HG03066 | Known Genes | | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3644996
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
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