Variant DetailsVariant: esv3404428 Internal ID | 14904704 | Landmark | | Location Information | | Cytoband | 13q14.2 | Allele length | Assembly | Allele length | hg38 | 89 | hg19 | 89 | hg18 | 89 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv8960420, essv8960401, essv8960405, essv8960412, essv8960415, essv8960417, essv8960409, essv8960411, essv8960406, essv8960422, essv8960408, essv8960423, essv8960418, essv8960413, essv8960399, essv8960407, essv8960410, essv8960419, essv8960416, essv8960402, essv8960400, essv8960421, essv8960404 | Samples | NA18947, NA11995, NA18861, NA18508, NA18980, NA07346, NA19005, NA18944, NA18942, NA18916, NA07347, NA12287, NA18949, NA12156, NA12044, NA18951, NA18948, NA19225, NA18523, NA18517, NA19129, NA12776, NA18965 | Known Genes | CAB39L | Method | Sequencing | Analysis | | Platform | Illumina | Comments | | Reference | 1000_Genomes_Consortium_Pilot_Project | Pubmed ID | 20981092 | Accession Number(s) | esv3404428
| Frequency | Sample Size | 185 | Observed Gain | 23 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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