Variant DetailsVariant: esv3417021Internal ID | 14917293 | Landmark | | Location Information | | Cytoband | 1q21.3 | Allele length | Assembly | Allele length | hg38 | 249 | hg19 | 249 | hg18 | 249 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv8673773, essv8673774 | Samples | NA19238, NA19240 | Known Genes | NUP210L | Method | Sequencing | Analysis | | Platform | Illumina | Comments | | Reference | 1000_Genomes_Consortium_Pilot_Project | Pubmed ID | 20981092 | Accession Number(s) | esv3417021
| Frequency | Sample Size | 185 | Observed Gain | 2 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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