Variant DetailsVariant: esv2720476Internal ID | 9954772 | Landmark | | Location Information | | Cytoband | 2q12.1 | Allele length | Assembly | Allele length | hg38 | 286 | hg19 | 286 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6955352, essv6880673, essv6669536, essv6847579, essv6853766, essv6886243, essv6859591, essv6675549, essv6686447, essv6846976, essv6906460, essv6726195 | Samples | SSM046, SSM011, SSM087, SSM088, SSM096, SSM026, SSM035, SSM094, SSM032, SSM031, SSM014, SSM086 | Known Genes | MRPS9 | 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) | esv2720476
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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