Variant DetailsVariant: esv3356630Internal ID | 14856893 | Landmark | | Location Information | | Cytoband | 5p13.3 | Allele length | Assembly | Allele length | hg38 | 6039 | hg19 | 6039 | hg18 | 6039 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv8923962, essv8923965, essv8923957, essv8923954, essv8923964, essv8923956, essv8923961, essv8923963, essv8923960, essv8923966, essv8923959, essv8923955 | Samples | NA12717, NA18563, NA19005, NA18558, NA18582, NA18571, NA18605, NA12489, NA12716, NA18961, NA07051, NA12763 | Known Genes | ADAMTS12 | Method | Sequencing | Analysis | | Platform | Illumina | Comments | | Reference | 1000_Genomes_Consortium_Pilot_Project | Pubmed ID | 20981092 | Accession Number(s) | esv3356630
| Frequency | Sample Size | 185 | Observed Gain | 12 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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