Variant DetailsVariant: esv3305066 Internal ID | 14805328 | Landmark | | Location Information | | Cytoband | 1q24.2 | Allele length | Assembly | Allele length | hg38 | 52 | hg19 | 52 | hg18 | 52 |
| Variant Type | CNV mobile element insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv7751367, essv7745727, essv7747490, essv7756792, essv7744387, essv7754318, essv7751760, essv7753768, essv7757559, essv7743429, essv7745881, essv7749120, essv7761555, essv7756463, essv7757944, essv7761213, essv7758955, essv7750036, essv7755750, essv7740724, essv7748364, essv7759302, essv7757173, essv7749743, essv7748184 | Samples | NA11881, NA12154, NA19093, NA11918, NA12828, NA12776, NA12044, NA18912, NA18508, NA11894, NA12144, NA12751, NA12006, NA19129, NA19238, NA18558, NA18945, NA18940, NA12749, NA12156, NA11830, NA12045, NA19240, NA18532, NA07000 | Known Genes | PRRX1 | Method | Sequencing | Analysis | | Platform | Illumina | Comments | | Reference | 1000_Genomes_Consortium_Pilot_Project | Pubmed ID | 20981092 | Accession Number(s) | esv3305066
| Frequency | Sample Size | 185 | Observed Gain | 25 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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