Fig. 2
From: Genotype–phenotype correlation in two Polish neonates with alveolar capillary dysplasia
Results of array CGH analyses. a Schematic representation of genes mapping within the 16q24.1 (hg19) interval, including FOXF1, FENDRR, LINC01081 and LINC01082 (pink rectangles). b Array CGH plot showing an ~ 1.45 Mb CNV deletion in Patient 1, involving the FOXF1 gene, its upstream enhancer (LINC01082, LINC01082), and IRF8, LINC00917, FENDRR, MTHFSD, FOXC2, and FOXL1. c Array CGH plot showing an ~ 0.7 Mb CNV deletion in Patient 2, involving the upstream FOXF1 enhancer (LINC01082 and LINC01082), COX411, IRF8, LINC00917, and leaving the FENDRR and FOXF1 genes intact