Variant DetailsVariant: essv15571334Internal ID | 5573150 | Landmark | | Location Information | | Cytoband | 17p13.3 | Allele length | Assembly | Allele length | hg38 | 470445 | hg19 | 523894 |
| Variant Type | CNV gain | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3639625 | Supporting Variants | | Samples | NA20318 | Known Genes | DBIL5P, FAM101B, FAM57A, GEMIN4, GLOD4, NXN, RNMTL1, VPS53 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | essv15571334
| Frequency | Sample Size | 2504 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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