Figure 1From: Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance Array CGH diagnostic service workflow. This example illustrates the diagnostic workflow for two patients, one of whom has a previously undetected imbalance of potential clinical significance. Yellow shading signifies automated procedures (we plan to also automate labelling, hybridisation and washing).Back to article page