Variant DetailsVariant: esv3386964Internal ID | 14887246 | Landmark | | Location Information | | Cytoband | 15q25.3 | Allele length | Assembly | Allele length | hg38 | 263 | hg19 | 263 | hg18 | 263 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv8969332, essv8969327, essv8969330, essv8969335, essv8969328, essv8969331, essv8969329, essv8969334, essv8969333, essv8969326 | Samples | NA18504, NA18510, NA18489, NA19138, NA18499, NA18853, NA18523, NA19147, NA18517, NA19116 | Known Genes | NTRK3 | Method | Sequencing | Analysis | | Platform | Illumina | Comments | | Reference | 1000_Genomes_Consortium_Pilot_Project | Pubmed ID | 20981092 | Accession Number(s) | esv3386964
| Frequency | Sample Size | 185 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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