Variant DetailsVariant: esv3644998Internal ID | 6685061 | Landmark | | Location Information | | Cytoband | 20p13 | Allele length | Assembly | Allele length | hg38 | 541973 | hg19 | 541973 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv16119035 | Samples | NA19454 | Known Genes | IDH3B, MIR1292, NOP56, SNORA51, SNORD110, SNORD119, SNORD56, SNORD57, SNORD86, SNRPB, TGM3, TGM6, TMC2, ZNF343 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3644998
| Frequency | Sample Size | 2504 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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