Variant DetailsVariant: essv8695256Internal ID | 14670539 | Landmark | | Location Information | | Cytoband | 6p21.32 | Allele length | Assembly | Allele length | hg38 | 2899 | hg19 | 2899 | hg18 | 2899 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | 1 | Merged Status | S | Merged Variants | esv3358357 | Supporting Variants | | Samples | NA19238 | Known Genes | C4A, C4B, C4B_2 | Method | Sequencing | Analysis | | Platform | Illumina | Comments | | Reference | 1000_Genomes_Consortium_Pilot_Project | Pubmed ID | 20981092 | Accession Number(s) | essv8695256
| Frequency | Sample Size | 185 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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