Variant DetailsVariant: essv8926794Internal ID | 14042261 | Landmark | | Location Information | | Cytoband | 5q31.3 | Allele length | Assembly | Allele length | hg38 | 169 | hg19 | 169 | hg18 | 169 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3422812 | Supporting Variants | | Samples | NA18870 | Known Genes | PCDHGA1, PCDHGA2, PCDHGA3, PCDHGA4, PCDHGA5, PCDHGA6, PCDHGA7, PCDHGA8, PCDHGA9, PCDHGB1, PCDHGB2, PCDHGB3, PCDHGB4, PCDHGB5 | Method | Sequencing | Analysis | | Platform | Illumina | Comments | | Reference | 1000_Genomes_Consortium_Pilot_Project | Pubmed ID | 20981092 | Accession Number(s) | essv8926794
| Frequency | Sample Size | 185 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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