Fig. 3From: Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarrayComparison of genome wide subchromosomal CNV sizes and breakpoints between array and cfDNA reported findings. A Size comparison for cfDNA (x-axis) and microarray (y-axis) detected and reported CNVs. B Precision of the start and end genomic coordinates of CNVs detected by cfDNA relative to the array defined start and end CNV genomic coordinates. NIPT = noninvasive prenatal testing, bp = base pairs, CNV = copy number variant, kbp = kilo base pairsBack to article page