Fig. 3From: Novel maternal duplication of 6p22.3-p25.3 with subtelomeric 6p25.3 deletion: new clinical findings and genotype–phenotype correlationsGenetic analysis of the proband. A Chromosome karyotype; B CNV-seq result showed a 20.88 Mb heterozygous duplication at 6p25.3-p22.3 and a 0.66 Mb heterozygous deletion at 6p25.3; C WES-CNV revealeda 0.3-Mb heterozygous deletion at 6p25.3 and a 20.49-Mb heterozygous duplication at 6p25.3-p22.3Back to article page