We offer high-resolution genome-wide microarrays for prenatal and postnatal analysis of genomic imbalances and Copy Number Variations (CNVs).
Array-CGH (Comparative Genomic Hybridisation) is an efficient and sensitive method for molecular cytogenetics that enables the detection of deletions and duplications in all genomic regions. The resolution limit of array-CGH exceeds by far that of conventional cytogenetics.
We offer all formats of array-CGH ranging from low to very high resolution specialized array designs.
Our laboratory is fully accredited for array-CGH and we regularly carry out external validation studies (EMQN). Pränatal-Medizin München has over 10 years of experience in Array-CGH.
In addition we also offer conventional cytogenetic analysis.
Deletion-830-kb-in-17q21.31 
