Variant DetailsVariant: esv3626839Internal ID | 6666987 | Landmark | | Location Information | | Cytoband | 11q13.4 | Allele length | Assembly | Allele length | hg38 | 511821 | hg19 | 511821 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv209e214 | Supporting Variants | essv14213953 | Samples | NA18582 | Known Genes | CHRDL2, KCNE3, LIPT2, MIR4696, PGM2L1, POLD3, RNF169 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3626839
| Frequency | Sample Size | 2504 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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