DNA Copy Number VariationsGene DosageAdenomatoid TumorOligonucleotide Array Sequence AnalysisComparative Genomic HybridizationGenome, HumanGenetic VariationPolymorphism, Single NucleotideGene DuplicationChromosome AberrationsGenomicsSegmental Duplications, GenomicNucleic Acid HybridizationSequence Analysis, DNAGenome-Wide Association StudyGenomeChromosomes, Artificial, BacterialGene AmplificationChromosomes, HumanDNA, NeoplasmGenotypeIn Situ Hybridization, FluorescenceChromosome MappingAlgorithmsPolymerase Chain ReactionGene Expression ProfilingGenetic Predisposition to DiseaseGenomic Structural VariationGene DeletionGenetic LociHereditary Breast and Ovarian Cancer SyndromePhenotypeDNA, MitochondrialChromosome DuplicationBase SequenceGenotyping TechniquesAllelesModels, GeneticSoftwareChromosome DeletionChromosomes, Human, Pair 1Reproducibility of ResultsDNA46, XX Disorders of Sex DevelopmentDatabases, GeneticChromosomes, Human, Pair 8Markov ChainsChromosomes, MammalianGenes, NeoplasmExomeLoss of HeterozygosityCluster AnalysisMutationMolecular Sequence DataAutistic DisorderGenetics, PopulationKaryotypingHapMap ProjectHaplotypesChromosomes, Human, Pair 16INDEL MutationCase-Control StudiesChromosomes, Human, Pair 22Chromosomes, Human, XHigh-Throughput Nucleotide SequencingNucleic Acid Amplification TechniquesAsian Continental Ancestry GroupGene Expression Regulation, NeoplasticSequence DeletionReal-Time Polymerase Chain ReactionGenomic InstabilityGenetic Association StudiesEvolution, MolecularAneuploidyComputational BiologyGene FrequencyChromosomes, Human, Pair 2Microarray AnalysisChromosomes, Human, Pair 6Chromosomes, Human, Pair 20Chromosomes, Human, Pair 17PedigreeInheritance PatternsHypertrichosisCell Line, TumorSmith-Magenis SyndromeDNA, ViralPseudogenesComplement C4abeta-DefensinsSpecies SpecificityDNA Mutational AnalysisBlotting, SouthwesternPolymorphism, GeneticChromosomesPan troglodytesNeoplasmsEuropean Continental Ancestry GroupPhylogenyChromosomes, Human, Pair 7