Variant DetailsVariant: esv2721738Internal ID | 9956036 | Landmark | | Location Information | | Cytoband | 2q37.3 | Allele length | Assembly | Allele length | hg38 | 321 | hg19 | 321 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6872094, essv6789660, essv6951047, essv6793792, essv6853974, essv6875081, essv6847791, essv6722456 | Samples | SSM071, SSM045, SSM087, SSM092, SSM086, SSM091, SSM070, SSM025 | Known Genes | LRRFIP1 | 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) | esv2721738
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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