Variant DetailsVariant: esv2724062Internal ID | 9958363 | Landmark | | Location Information | | Cytoband | 1q42.13 | Allele length | Assembly | Allele length | hg38 | 1728 | hg19 | 1728 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6859408, essv6720187, essv6961828, essv6918240, essv6697121, essv6878320, essv6742292, essv6886121, essv6786209, essv6747930, essv6670632, essv6829171 | Samples | SSM027, SSM038, SSM009, SSM088, SSM096, SSM003, SSM081, SSM007, SSM053, SSM005, SSM056, SSM012 | Known Genes | ADCK3 | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | esv2724062
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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