Variant CNV_M1_HG19_7_146133366_146139492
Location: chr7:146133366-146139492 (6.1Kb)
Site classification: Multi-allelic
Variant DCN frequency: 0.031
Genes Overlapped
Site classification: Multi-allelic
Variant DCN frequency: 0.031
Genes Overlapped
CNTNAP2 | INTRON | contactin-associated protein-like 2 precursor |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2 CN3 ASW 0 3 42 0 CEU 0 0 66 0 CHB 0 0 78 0 CHS 0 0 91 0 CLM 0 1 48 0 FIN 0 0 62 0 GBR 0 0 53 1 IBS 0 0 6 0 JPT 0 0 69 0 LWK 0 8 61 0 MXL 0 1 53 0 PUR 0 0 52 0 TSI 0 0 83 0 YRI 0 13 58 0 AFR 0 21 119 0 AFR+ 0 24 161 0 AMR 0 2 153 0 ASN 0 0 238 0 EUR 0 0 270 1 ALL 0 26 822 1
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2 CN3 ASW 0 3 42 0 CEU 0 0 66 0 CHB 0 0 78 0 CHS 0 0 91 0 CLM 0 1 48 0 FIN 0 0 62 0 GBR 0 0 53 1 IBS 0 0 6 0 JPT 0 0 68 0 LWK 0 8 61 0 MXL 0 1 53 0 PUR 0 0 51 0 TSI 0 0 83 0 YRI 0 12 58 0 AFR 0 20 119 0 AFR+ 0 23 161 0 AMR 0 2 152 0 ASN 0 0 237 0 EUR 0 0 270 1 ALL 0 25 820 1
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI